Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives

The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the...
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Gespeichert in:

Autor*in:	BOGDAN COMANITA [verfasserIn] IRINA POPOVICI [verfasserIn] EUGENIA COMANITA [verfasserIn] GHEORGHE ROMAN [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2001

Schlagwörter:	ortho-phenolic ketones Mannich bases amine exchange reaction Mannich bases oximes

Übergeordnetes Werk:	In: Journal of the Serbian Chemical Society - Serbian Chemical Society, 2017, 66(2001), 1, Seite 9-16
Übergeordnetes Werk:	volume:66 ; year:2001 ; number:1 ; pages:9-16

Links:	Link aufrufen Link aufrufen Journal toc

Katalog-ID:	DOAJ065790332

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allfields	(DE-627)DOAJ065790332 (DE-599)DOAJ8185fa460b4d4e5d9951c3f0e279999d DE-627 ger DE-627 rakwb eng QD1-999 BOGDAN COMANITA verfasserin aut Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives 2001 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH. ortho-phenolic ketones Mannich bases amine exchange reaction Mannich bases oximes Chemistry IRINA POPOVICI verfasserin aut EUGENIA COMANITA verfasserin aut GHEORGHE ROMAN verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 66(2001), 1, Seite 9-16 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:66 year:2001 number:1 pages:9-16 https://doaj.org/article/8185fa460b4d4e5d9951c3f0e279999d kostenfrei http://www.shd.org.yu/HtDocs/SHD/Vol66/No1/V66-no1-02.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_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2014 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 66 2001 1 9-16
spelling	(DE-627)DOAJ065790332 (DE-599)DOAJ8185fa460b4d4e5d9951c3f0e279999d DE-627 ger DE-627 rakwb eng QD1-999 BOGDAN COMANITA verfasserin aut Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives 2001 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH. ortho-phenolic ketones Mannich bases amine exchange reaction Mannich bases oximes Chemistry IRINA POPOVICI verfasserin aut EUGENIA COMANITA verfasserin aut GHEORGHE ROMAN verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 66(2001), 1, Seite 9-16 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:66 year:2001 number:1 pages:9-16 https://doaj.org/article/8185fa460b4d4e5d9951c3f0e279999d kostenfrei http://www.shd.org.yu/HtDocs/SHD/Vol66/No1/V66-no1-02.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_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2014 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 66 2001 1 9-16
allfields_unstemmed	(DE-627)DOAJ065790332 (DE-599)DOAJ8185fa460b4d4e5d9951c3f0e279999d DE-627 ger DE-627 rakwb eng QD1-999 BOGDAN COMANITA verfasserin aut Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives 2001 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH. ortho-phenolic ketones Mannich bases amine exchange reaction Mannich bases oximes Chemistry IRINA POPOVICI verfasserin aut EUGENIA COMANITA verfasserin aut GHEORGHE ROMAN verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 66(2001), 1, Seite 9-16 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:66 year:2001 number:1 pages:9-16 https://doaj.org/article/8185fa460b4d4e5d9951c3f0e279999d kostenfrei http://www.shd.org.yu/HtDocs/SHD/Vol66/No1/V66-no1-02.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_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2014 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 66 2001 1 9-16
allfieldsGer	(DE-627)DOAJ065790332 (DE-599)DOAJ8185fa460b4d4e5d9951c3f0e279999d DE-627 ger DE-627 rakwb eng QD1-999 BOGDAN COMANITA verfasserin aut Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives 2001 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH. ortho-phenolic ketones Mannich bases amine exchange reaction Mannich bases oximes Chemistry IRINA POPOVICI verfasserin aut EUGENIA COMANITA verfasserin aut GHEORGHE ROMAN verfasserin aut In Journal of the Serbian Chemical Society Serbian Chemical Society, 2017 66(2001), 1, Seite 9-16 (DE-627)324742363 (DE-600)2030173-X 18207421 nnns volume:66 year:2001 number:1 pages:9-16 https://doaj.org/article/8185fa460b4d4e5d9951c3f0e279999d kostenfrei http://www.shd.org.yu/HtDocs/SHD/Vol66/No1/V66-no1-02.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_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2014 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 66 2001 1 9-16
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author	BOGDAN COMANITA
spellingShingle	BOGDAN COMANITA misc QD1-999 misc ortho-phenolic ketones misc Mannich bases misc amine exchange reaction misc Mannich bases oximes misc Chemistry Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
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topic_title	QD1-999 Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives ortho-phenolic ketones Mannich bases amine exchange reaction Mannich bases oximes
topic	misc QD1-999 misc ortho-phenolic ketones misc Mannich bases misc amine exchange reaction misc Mannich bases oximes misc Chemistry
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title	Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
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title_full	Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
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title_sort	synthesis and reactivity of some mannich bases. viii. studies on several mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
callnumber	QD1-999
title_auth	Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
abstract	The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH.
abstractGer	The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH.
abstract_unstemmed	The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10 % NaOH.
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title_short	Synthesis and reactivity of some Mannich bases. VIII. Studies on several Mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
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