Synthesis of 2-azetidinones substituted quinoline derivative

Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-a...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Mashelkar Uday C. [verfasserIn] Jha Mukesh S. [verfasserIn] Mashelkar Beena U. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2013

Schlagwörter:	acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone

Übergeordnetes Werk:	In: Journal of the Serbian Chemical Society - Serbian Chemical Society, 2017, 78(2013), 5, Seite 621-625
Übergeordnetes Werk:	volume:78 ; year:2013 ; number:5 ; pages:621-625

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.2298/JSC120617081M

Katalog-ID:	DOAJ054387280

Internformat


LEADER	01000caa a22002652 4500
001	DOAJ054387280
003	DE-627
005	20230503015303.0
007	cr uuu---uuuuu
008	230227s2013 xx \|\|\|\|\|o 00\| \|\|eng c
024	7		\|a 10.2298/JSC120617081M \|2 doi
035			\|a (DE-627)DOAJ054387280
035			\|a (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157
040			\|a DE-627 \|b ger \|c DE-627 \|e rakwb
041			\|a eng
050		0	\|a QD1-999
100	0		\|a Mashelkar Uday C. \|e verfasserin \|4 aut
245	1	0	\|a Synthesis of 2-azetidinones substituted quinoline derivative
264		1	\|c 2013
336			\|a Text \|b txt \|2 rdacontent
337			\|a Computermedien \|b c \|2 rdamedia
338			\|a Online-Ressource \|b cr \|2 rdacarrier
520			\|a Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones.
650		4	\|a acetanilide
650		4	\|a 2-chloro-3-formyl quinoline
650		4	\|a aromatic amine
650		4	\|a acid chloride
650		4	\|a tri-n-butylamine
650		4	\|a 2-azetidinone
653		0	\|a Chemistry
700	0		\|a Jha Mukesh S. \|e verfasserin \|4 aut
700	0		\|a Mashelkar Beena U. \|e verfasserin \|4 aut
773	0	8	\|i In \|t Journal of the Serbian Chemical Society \|d Serbian Chemical Society, 2017 \|g 78(2013), 5, Seite 621-625 \|w (DE-627)324742363 \|w (DE-600)2030173-X \|x 18207421 \|7 nnns
773	1	8	\|g volume:78 \|g year:2013 \|g number:5 \|g pages:621-625
856	4	0	\|u https://doi.org/10.2298/JSC120617081M \|z kostenfrei
856	4	0	\|u https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 \|z kostenfrei
856	4	0	\|u http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf \|z kostenfrei
856	4	2	\|u https://doaj.org/toc/0352-5139 \|y Journal toc \|z kostenfrei
912			\|a GBV_USEFLAG_A
912			\|a SYSFLAG_A
912			\|a GBV_DOAJ
912			\|a SSG-OLC-PHA
912			\|a GBV_ILN_20
912			\|a GBV_ILN_22
912			\|a GBV_ILN_23
912			\|a GBV_ILN_24
912			\|a GBV_ILN_39
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_73
912			\|a GBV_ILN_95
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_151
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_206
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_4012
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4126
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4367
912			\|a GBV_ILN_4700
951			\|a AR
952			\|d 78 \|j 2013 \|e 5 \|h 621-625

Indexfelder

author_variant	m u c muc j m s jms m b u mbu
matchkey_str	article:18207421:2013----::yteio2ztdnnsusiueqi
hierarchy_sort_str	2013
callnumber-subject-code	QD
publishDate	2013
allfields	10.2298/JSC120617081M doi (DE-627)DOAJ054387280 (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157 DE-627 ger DE-627 rakwb eng QD1-999 Mashelkar Uday C. verfasserin aut Synthesis of 2-azetidinones substituted quinoline derivative 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone Chemistry Jha Mukesh S. verfasserin aut Mashelkar Beena U. verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 78(2013), 5, Seite 621-625 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:78 year:2013 number:5 pages:621-625 https://doi.org/10.2298/JSC120617081M kostenfrei https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 kostenfrei http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf kostenfrei https://doaj.org/toc/0352-5139 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 78 2013 5 621-625
spelling	10.2298/JSC120617081M doi (DE-627)DOAJ054387280 (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157 DE-627 ger DE-627 rakwb eng QD1-999 Mashelkar Uday C. verfasserin aut Synthesis of 2-azetidinones substituted quinoline derivative 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone Chemistry Jha Mukesh S. verfasserin aut Mashelkar Beena U. verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 78(2013), 5, Seite 621-625 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:78 year:2013 number:5 pages:621-625 https://doi.org/10.2298/JSC120617081M kostenfrei https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 kostenfrei http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf kostenfrei https://doaj.org/toc/0352-5139 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 78 2013 5 621-625
allfields_unstemmed	10.2298/JSC120617081M doi (DE-627)DOAJ054387280 (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157 DE-627 ger DE-627 rakwb eng QD1-999 Mashelkar Uday C. verfasserin aut Synthesis of 2-azetidinones substituted quinoline derivative 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone Chemistry Jha Mukesh S. verfasserin aut Mashelkar Beena U. verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 78(2013), 5, Seite 621-625 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:78 year:2013 number:5 pages:621-625 https://doi.org/10.2298/JSC120617081M kostenfrei https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 kostenfrei http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf kostenfrei https://doaj.org/toc/0352-5139 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 78 2013 5 621-625
allfieldsGer	10.2298/JSC120617081M doi (DE-627)DOAJ054387280 (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157 DE-627 ger DE-627 rakwb eng QD1-999 Mashelkar Uday C. verfasserin aut Synthesis of 2-azetidinones substituted quinoline derivative 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone Chemistry Jha Mukesh S. verfasserin aut Mashelkar Beena U. verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 78(2013), 5, Seite 621-625 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:78 year:2013 number:5 pages:621-625 https://doi.org/10.2298/JSC120617081M kostenfrei https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 kostenfrei http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf kostenfrei https://doaj.org/toc/0352-5139 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 78 2013 5 621-625
allfieldsSound	10.2298/JSC120617081M doi (DE-627)DOAJ054387280 (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157 DE-627 ger DE-627 rakwb eng QD1-999 Mashelkar Uday C. verfasserin aut Synthesis of 2-azetidinones substituted quinoline derivative 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones. acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone Chemistry Jha Mukesh S. verfasserin aut Mashelkar Beena U. verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 78(2013), 5, Seite 621-625 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:78 year:2013 number:5 pages:621-625 https://doi.org/10.2298/JSC120617081M kostenfrei https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 kostenfrei http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf kostenfrei https://doaj.org/toc/0352-5139 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 78 2013 5 621-625
language	English
source	In Journal of the Serbian Chemical Society 78(2013), 5, Seite 621-625 volume:78 year:2013 number:5 pages:621-625
sourceStr	In Journal of the Serbian Chemical Society 78(2013), 5, Seite 621-625 volume:78 year:2013 number:5 pages:621-625
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone Chemistry
isfreeaccess_bool	true
container_title	Journal of the Serbian Chemical Society
authorswithroles_txt_mv	Mashelkar Uday C. @@aut@@ Jha Mukesh S. @@aut@@ Mashelkar Beena U. @@aut@@
publishDateDaySort_date	2013-01-01T00:00:00Z
hierarchy_top_id	324742363
id	DOAJ054387280
language_de	englisch
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ054387280</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503015303.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230227s2013 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.2298/JSC120617081M</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ054387280</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QD1-999</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Mashelkar Uday C.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis of 2-azetidinones substituted quinoline derivative</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2013</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">acetanilide</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">2-chloro-3-formyl quinoline</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">aromatic amine</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">acid chloride</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">tri-n-butylamine</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">2-azetidinone</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Chemistry</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Jha Mukesh S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Mashelkar Beena U.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Journal of the Serbian Chemical Society</subfield><subfield code="d">Serbian Chemical Society, 2017</subfield><subfield code="g">78(2013), 5, Seite 621-625</subfield><subfield code="w">(DE-627)324742363</subfield><subfield code="w">(DE-600)2030173-X</subfield><subfield code="x">18207421</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:78</subfield><subfield code="g">year:2013</subfield><subfield code="g">number:5</subfield><subfield code="g">pages:621-625</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.2298/JSC120617081M</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/0352-5139</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_170</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_206</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_370</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2005</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2009</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2011</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2027</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2055</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2111</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">78</subfield><subfield code="j">2013</subfield><subfield code="e">5</subfield><subfield code="h">621-625</subfield></datafield></record></collection>
callnumber-first	Q - Science
author	Mashelkar Uday C.
spellingShingle	Mashelkar Uday C. misc QD1-999 misc acetanilide misc 2-chloro-3-formyl quinoline misc aromatic amine misc acid chloride misc tri-n-butylamine misc 2-azetidinone misc Chemistry Synthesis of 2-azetidinones substituted quinoline derivative
authorStr	Mashelkar Uday C.
ppnlink_with_tag_str_mv	@@773@@(DE-627)324742363
format	electronic Article
delete_txt_mv	keep
author_role	aut aut aut
collection	DOAJ
remote_str	true
callnumber-label	QD1-999
illustrated	Not Illustrated
issn	18207421
topic_title	QD1-999 Synthesis of 2-azetidinones substituted quinoline derivative acetanilide 2-chloro-3-formyl quinoline aromatic amine acid chloride tri-n-butylamine 2-azetidinone
topic	misc QD1-999 misc acetanilide misc 2-chloro-3-formyl quinoline misc aromatic amine misc acid chloride misc tri-n-butylamine misc 2-azetidinone misc Chemistry
topic_unstemmed	misc QD1-999 misc acetanilide misc 2-chloro-3-formyl quinoline misc aromatic amine misc acid chloride misc tri-n-butylamine misc 2-azetidinone misc Chemistry
topic_browse	misc QD1-999 misc acetanilide misc 2-chloro-3-formyl quinoline misc aromatic amine misc acid chloride misc tri-n-butylamine misc 2-azetidinone misc Chemistry
format_facet	Elektronische Aufsätze Aufsätze Elektronische Ressource
format_main_str_mv	Text Zeitschrift/Artikel
carriertype_str_mv	cr
hierarchy_parent_title	Journal of the Serbian Chemical Society
hierarchy_parent_id	324742363
hierarchy_top_title	Journal of the Serbian Chemical Society
isfreeaccess_txt	true
familylinks_str_mv	(DE-627)324742363 (DE-600)2030173-X
title	Synthesis of 2-azetidinones substituted quinoline derivative
ctrlnum	(DE-627)DOAJ054387280 (DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157
title_full	Synthesis of 2-azetidinones substituted quinoline derivative
author_sort	Mashelkar Uday C.
journal	Journal of the Serbian Chemical Society
journalStr	Journal of the Serbian Chemical Society
callnumber-first-code	Q
lang_code	eng
isOA_bool	true
recordtype	marc
publishDateSort	2013
contenttype_str_mv	txt
container_start_page	621
author_browse	Mashelkar Uday C. Jha Mukesh S. Mashelkar Beena U.
container_volume	78
class	QD1-999
format_se	Elektronische Aufsätze
author-letter	Mashelkar Uday C.
doi_str_mv	10.2298/JSC120617081M
author2-role	verfasserin
title_sort	synthesis of 2-azetidinones substituted quinoline derivative
callnumber	QD1-999
title_auth	Synthesis of 2-azetidinones substituted quinoline derivative
abstract	Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones.
abstractGer	Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones.
abstract_unstemmed	Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones.
collection_details	GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700
container_issue	5
title_short	Synthesis of 2-azetidinones substituted quinoline derivative
url	https://doi.org/10.2298/JSC120617081M https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157 http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf https://doaj.org/toc/0352-5139
remote_bool	true
author2	Jha Mukesh S. Mashelkar Beena U.
author2Str	Jha Mukesh S. Mashelkar Beena U.
ppnlink	324742363
callnumber-subject	QD - Chemistry
mediatype_str_mv	c
isOA_txt	true
hochschulschrift_bool	false
doi_str	10.2298/JSC120617081M
callnumber-a	QD1-999
up_date	2024-07-03T22:52:07.262Z
_version_	1803600136515878912
fullrecord_marcxml	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ054387280</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230503015303.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230227s2013 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.2298/JSC120617081M</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ054387280</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJb49e3ea4940a4ac0abd5bfb7e4acf157</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QD1-999</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Mashelkar Uday C.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis of 2-azetidinones substituted quinoline derivative</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2013</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Acetanilide is converted into 2-chloro-3-formyl quinoline by reacting with DMF-POCl3 at 80-90ºC and then condensed with aromatic primary amines to give Schiff bases (3a-3c). These Schiff bases are then reacted with acid chlorides in the presence of base in toluene to give 1, 3, 4-substituted 2-azetidinones.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">acetanilide</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">2-chloro-3-formyl quinoline</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">aromatic amine</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">acid chloride</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">tri-n-butylamine</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">2-azetidinone</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Chemistry</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Jha Mukesh S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Mashelkar Beena U.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Journal of the Serbian Chemical Society</subfield><subfield code="d">Serbian Chemical Society, 2017</subfield><subfield code="g">78(2013), 5, Seite 621-625</subfield><subfield code="w">(DE-627)324742363</subfield><subfield code="w">(DE-600)2030173-X</subfield><subfield code="x">18207421</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:78</subfield><subfield code="g">year:2013</subfield><subfield code="g">number:5</subfield><subfield code="g">pages:621-625</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.2298/JSC120617081M</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/b49e3ea4940a4ac0abd5bfb7e4acf157</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200081M.pdf</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/0352-5139</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_170</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_206</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_224</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_370</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2005</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2009</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2011</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2027</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2055</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2111</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">78</subfield><subfield code="j">2013</subfield><subfield code="e">5</subfield><subfield code="h">621-625</subfield></datafield></record></collection>
score	7.3995867

Nicht das Richtige dabei?

Schreiben Sie uns!

Synthesis of 2-azetidinones substituted quinoline derivative

Nicht das Richtige dabei?

Zugang & Verfügbarkeit

Vorhandene Bände

Nicht das Richtige dabei?