Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization

Gespeichert in:

Autor*in:	Paquette, Leo A. [verfasserIn] Deaton, David N. [verfasserIn] Endo, Yasuyuki [verfasserIn] Poupart, Marc Andre

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	s.l.: American Chemical Society ; 1993

Umfang:	12

Reproduktion:	ACS Legacy Archives
Übergeordnetes Werk:	In: The journal of organic chemistry - [S.l.] : American Chemical Society, 1936, 58(1993), 16, Seite 4262-4273
Übergeordnetes Werk:	volume:58 ; year:1993 ; number:16 ; pages:4262-4273 ; extent:12

Links:	Link aufrufen

DOI / URN:	10.1021/jo00068a021

Katalog-ID:	NLEJ221291091

Internformat


LEADER	01000caa a22002652 4500
001	NLEJ221291091
003	DE-627
005	20210705200241.0
007	cr uuu---uuuuu
008	090824s1993 xx \|\|\|\|\|o 00\| \|\|eng c
024	7		\|a 10.1021/jo00068a021 \|2 doi
035			\|a (DE-627)NLEJ221291091
040			\|a DE-627 \|b ger \|c DE-627 \|e rakwb
041			\|a eng
100	1		\|a Paquette, Leo A. \|e verfasserin \|4 aut
245	1	0	\|a Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
264		1	\|a s.l. \|b American Chemical Society \|c 1993
300			\|a 12
336			\|a nicht spezifiziert \|b zzz \|2 rdacontent
337			\|a nicht spezifiziert \|b z \|2 rdamedia
338			\|a nicht spezifiziert \|b zu \|2 rdacarrier
533			\|f ACS Legacy Archives
700	1		\|a Deaton, David N. \|e verfasserin \|4 aut
700	1		\|a Endo, Yasuyuki \|e verfasserin \|4 aut
700	1		\|a Poupart, Marc Andre \|4 oth
773	0	8	\|i In \|t The journal of organic chemistry \|d [S.l.] : American Chemical Society, 1936 \|g 58(1993), 16, Seite 4262-4273 \|h Online-Ressource \|w (DE-627)NLEJ220026254 \|w (DE-600)1472273-2 \|x 1520-6904 \|7 nnns
773	1	8	\|g volume:58 \|g year:1993 \|g number:16 \|g pages:4262-4273 \|g extent:12
856	4	0	\|u http://dx.doi.org/10.1021/jo00068a021
912			\|a GBV_USEFLAG_U
912			\|a ZDB-1-ACS
912			\|a GBV_NL_ARTICLE
951			\|a AR
952			\|d 58 \|j 1993 \|e 16 \|h 4262-4273 \|g 12

Indexfelder

author_variant	l a p la lap d n d dn dnd y e ye
matchkey_str	article:15206904:1993----::tdedrcetwrteoasnhssfeoueiaiiiaovretnnislcieprahnovnnwra
hierarchy_sort_str	1993
publishDate	1993
allfields	10.1021/jo00068a021 doi (DE-627)NLEJ221291091 DE-627 ger DE-627 rakwb eng Paquette, Leo A. verfasserin aut Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization s.l. American Chemical Society 1993 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier ACS Legacy Archives Deaton, David N. verfasserin aut Endo, Yasuyuki verfasserin aut Poupart, Marc Andre oth In The journal of organic chemistry [S.l.] : American Chemical Society, 1936 58(1993), 16, Seite 4262-4273 Online-Ressource (DE-627)NLEJ220026254 (DE-600)1472273-2 1520-6904 nnns volume:58 year:1993 number:16 pages:4262-4273 extent:12 http://dx.doi.org/10.1021/jo00068a021 GBV_USEFLAG_U ZDB-1-ACS GBV_NL_ARTICLE AR 58 1993 16 4262-4273 12
spelling	10.1021/jo00068a021 doi (DE-627)NLEJ221291091 DE-627 ger DE-627 rakwb eng Paquette, Leo A. verfasserin aut Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization s.l. American Chemical Society 1993 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier ACS Legacy Archives Deaton, David N. verfasserin aut Endo, Yasuyuki verfasserin aut Poupart, Marc Andre oth In The journal of organic chemistry [S.l.] : American Chemical Society, 1936 58(1993), 16, Seite 4262-4273 Online-Ressource (DE-627)NLEJ220026254 (DE-600)1472273-2 1520-6904 nnns volume:58 year:1993 number:16 pages:4262-4273 extent:12 http://dx.doi.org/10.1021/jo00068a021 GBV_USEFLAG_U ZDB-1-ACS GBV_NL_ARTICLE AR 58 1993 16 4262-4273 12
allfields_unstemmed	10.1021/jo00068a021 doi (DE-627)NLEJ221291091 DE-627 ger DE-627 rakwb eng Paquette, Leo A. verfasserin aut Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization s.l. American Chemical Society 1993 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier ACS Legacy Archives Deaton, David N. verfasserin aut Endo, Yasuyuki verfasserin aut Poupart, Marc Andre oth In The journal of organic chemistry [S.l.] : American Chemical Society, 1936 58(1993), 16, Seite 4262-4273 Online-Ressource (DE-627)NLEJ220026254 (DE-600)1472273-2 1520-6904 nnns volume:58 year:1993 number:16 pages:4262-4273 extent:12 http://dx.doi.org/10.1021/jo00068a021 GBV_USEFLAG_U ZDB-1-ACS GBV_NL_ARTICLE AR 58 1993 16 4262-4273 12
allfieldsGer	10.1021/jo00068a021 doi (DE-627)NLEJ221291091 DE-627 ger DE-627 rakwb eng Paquette, Leo A. verfasserin aut Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization s.l. American Chemical Society 1993 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier ACS Legacy Archives Deaton, David N. verfasserin aut Endo, Yasuyuki verfasserin aut Poupart, Marc Andre oth In The journal of organic chemistry [S.l.] : American Chemical Society, 1936 58(1993), 16, Seite 4262-4273 Online-Ressource (DE-627)NLEJ220026254 (DE-600)1472273-2 1520-6904 nnns volume:58 year:1993 number:16 pages:4262-4273 extent:12 http://dx.doi.org/10.1021/jo00068a021 GBV_USEFLAG_U ZDB-1-ACS GBV_NL_ARTICLE AR 58 1993 16 4262-4273 12
allfieldsSound	10.1021/jo00068a021 doi (DE-627)NLEJ221291091 DE-627 ger DE-627 rakwb eng Paquette, Leo A. verfasserin aut Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization s.l. American Chemical Society 1993 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier ACS Legacy Archives Deaton, David N. verfasserin aut Endo, Yasuyuki verfasserin aut Poupart, Marc Andre oth In The journal of organic chemistry [S.l.] : American Chemical Society, 1936 58(1993), 16, Seite 4262-4273 Online-Ressource (DE-627)NLEJ220026254 (DE-600)1472273-2 1520-6904 nnns volume:58 year:1993 number:16 pages:4262-4273 extent:12 http://dx.doi.org/10.1021/jo00068a021 GBV_USEFLAG_U ZDB-1-ACS GBV_NL_ARTICLE AR 58 1993 16 4262-4273 12
language	English
source	In The journal of organic chemistry 58(1993), 16, Seite 4262-4273 volume:58 year:1993 number:16 pages:4262-4273 extent:12
sourceStr	In The journal of organic chemistry 58(1993), 16, Seite 4262-4273 volume:58 year:1993 number:16 pages:4262-4273 extent:12
format_phy_str_mv	Article
institution	findex.gbv.de
isfreeaccess_bool	false
container_title	The journal of organic chemistry
authorswithroles_txt_mv	Paquette, Leo A. @@aut@@ Deaton, David N. @@aut@@ Endo, Yasuyuki @@aut@@ Poupart, Marc Andre @@oth@@
publishDateDaySort_date	1993-01-01T00:00:00Z
hierarchy_top_id	NLEJ220026254
id	NLEJ221291091
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">NLEJ221291091</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210705200241.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">090824s1993 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1021/jo00068a021</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ221291091</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="100" ind1="1" ind2=" "><subfield code="a">Paquette, Leo A.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">s.l.</subfield><subfield code="b">American Chemical Society</subfield><subfield code="c">1993</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">12</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">ACS Legacy Archives</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Deaton, David N.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Endo, Yasuyuki</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Poupart, Marc Andre</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">The journal of organic chemistry</subfield><subfield code="d">[S.l.] : American Chemical Society, 1936</subfield><subfield code="g">58(1993), 16, Seite 4262-4273</subfield><subfield code="h">Online-Ressource</subfield><subfield code="w">(DE-627)NLEJ220026254</subfield><subfield code="w">(DE-600)1472273-2</subfield><subfield code="x">1520-6904</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:58</subfield><subfield code="g">year:1993</subfield><subfield code="g">number:16</subfield><subfield code="g">pages:4262-4273</subfield><subfield code="g">extent:12</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1021/jo00068a021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-ACS</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">58</subfield><subfield code="j">1993</subfield><subfield code="e">16</subfield><subfield code="h">4262-4273</subfield><subfield code="g">12</subfield></datafield></record></collection>
series2	ACS Legacy Archives
author	Paquette, Leo A.
spellingShingle	Paquette, Leo A. Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
authorStr	Paquette, Leo A.
ppnlink_with_tag_str_mv	@@773@@(DE-627)NLEJ220026254
format	electronic Article
delete_txt_mv	keep
author_role	aut aut aut
collection	NL
publishPlace	s.l.
remote_str	true
illustrated	Not Illustrated
issn	1520-6904
topic_title	Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
publisher	American Chemical Society
publisherStr	American Chemical Society
format_facet	Elektronische Aufsätze Aufsätze Elektronische Ressource
format_main_str_mv	Text Zeitschrift/Artikel
carriertype_str_mv	zu
author2_variant	m a p ma map
hierarchy_parent_title	The journal of organic chemistry
hierarchy_parent_id	NLEJ220026254
hierarchy_top_title	The journal of organic chemistry
isfreeaccess_txt	false
familylinks_str_mv	(DE-627)NLEJ220026254 (DE-600)1472273-2
title	Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
ctrlnum	(DE-627)NLEJ221291091
title_full	Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
author_sort	Paquette, Leo A.
journal	The journal of organic chemistry
journalStr	The journal of organic chemistry
lang_code	eng
isOA_bool	false
recordtype	marc
publishDateSort	1993
contenttype_str_mv	zzz
container_start_page	4262
author_browse	Paquette, Leo A. Deaton, David N. Endo, Yasuyuki
container_volume	58
physical	12
format_se	Elektronische Aufsätze
author-letter	Paquette, Leo A.
doi_str_mv	10.1021/jo00068a021
author2-role	verfasserin
title_sort	studies directed toward the total synthesis of cerorubenic acid-iii. 3. a convergent enantioselective approach involving new arrangements for the actuation of ring d cyclization
title_auth	Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
collection_details	GBV_USEFLAG_U ZDB-1-ACS GBV_NL_ARTICLE
container_issue	16
title_short	Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization
url	http://dx.doi.org/10.1021/jo00068a021
remote_bool	true
author2	Deaton, David N. Endo, Yasuyuki Poupart, Marc Andre
author2Str	Deaton, David N. Endo, Yasuyuki Poupart, Marc Andre
ppnlink	NLEJ220026254
mediatype_str_mv	z
isOA_txt	false
hochschulschrift_bool	false
author2_role	oth
doi_str	10.1021/jo00068a021
up_date	2024-07-06T09:25:02.892Z
_version_	1803821150783930368
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">NLEJ221291091</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210705200241.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">090824s1993 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1021/jo00068a021</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ221291091</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="100" ind1="1" ind2=" "><subfield code="a">Paquette, Leo A.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">s.l.</subfield><subfield code="b">American Chemical Society</subfield><subfield code="c">1993</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">12</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">ACS Legacy Archives</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Deaton, David N.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Endo, Yasuyuki</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Poupart, Marc Andre</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">The journal of organic chemistry</subfield><subfield code="d">[S.l.] : American Chemical Society, 1936</subfield><subfield code="g">58(1993), 16, Seite 4262-4273</subfield><subfield code="h">Online-Ressource</subfield><subfield code="w">(DE-627)NLEJ220026254</subfield><subfield code="w">(DE-600)1472273-2</subfield><subfield code="x">1520-6904</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:58</subfield><subfield code="g">year:1993</subfield><subfield code="g">number:16</subfield><subfield code="g">pages:4262-4273</subfield><subfield code="g">extent:12</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1021/jo00068a021</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-ACS</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">58</subfield><subfield code="j">1993</subfield><subfield code="e">16</subfield><subfield code="h">4262-4273</subfield><subfield code="g">12</subfield></datafield></record></collection>
score	7.4000244

Nicht das Richtige dabei?

Schreiben Sie uns!

Studies directed toward the total synthesis of cerorubenic acid-III. 3. A convergent enantioselective approach involving new arrangements for the actuation of ring D cyclization

Nicht das Richtige dabei?

Zugang & Verfügbarkeit

Vorhandene Bände

Nicht das Richtige dabei?