About: "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent

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About: "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 2004

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) 2004 թվականին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в січні 2004 (uk) im Januar 2004 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2004 (ast) artikull shkencor i botuar më 01 janar 2004 (sq) scientific article published on 01 January 2004 (en)
publication date	wds:Q75261985-66CA3997-9B71-4AE2-8FDA-236BE86FF25C
publication date	2004-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q75261985-37933B45-E691-4C86-8FEE-0B9FFDEC7EDB wds:Q75261985-584CC090-82E9-4139-95FA-726FBD7C1A59
cites work	SNF4435C and D, Novel Immunosuppressants Produced by a Strain of Streptomyces spectabilis. II. Structure Elucidation. SNF4435C and D, novel immunosuppressants produced by a strain of Streptomyces spectabilis. I. Taxonomy, fermentation, isolation and biological activities.
author name string	wds:Q75261985-A589B5B3-5043-4654-958D-D9400C08E6D5
author name string	Yeon-Hee Lim
rdfs:label	"Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (en) "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (nl) "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (sq)
skos:prefLabel	"Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (en) "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (nl) "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (sq)
name	"Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (en) "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (nl) "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (sq)
author	wds:Q75261985-3F09B666-D36A-45C8-A3D7-17BBCFD09F66
author	Kathlyn A. Parker
title	wds:Q75261985-371E0A1C-FD0B-4E0C-90E1-72F2EC363BDE
title	"Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent (en)
page(s)	wds:Q75261985-E13853BC-8446-4AE5-9B64-5938DA1BA2A2
page(s)	161-164
instance of	wds:Q75261985-10AD6297-ED96-4A04-AA20-C6553DB83F85
instance of	scholarly article
PubMed ID	wds:Q75261985-B0EF5405-AC15-4C72-B203-088EAC11EA76
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14723518
PubMed ID	14723518
published in	wds:Q75261985-368E6DD5-25FD-4A9A-8E1A-A8D67442BAB4
published in	Organic Letters
issue	wds:Q75261985-BB3DED53-EBD2-457F-981B-4621428C9B12
volume	wds:Q75261985-36DE3B34-D9C0-4DEA-B24D-73CFAA75425F
issue	2
volume	6
DOI	wds:Q75261985-BBC1A8F2-9C62-49B9-8B60-EEE2FECAB844
DOI	http://dx.doi.org/10.1021/OL036048%2B
DOI	10.1021/OL036048+
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q75261985
is cites work of	Photochemical Origin of the Immunosuppressive SNF4435C/D and Formation of Orinocin through “Polyene Splicing” Total synthesis of kingianin A. The total synthesis of (-)-crispatene Total synthesis of the potent androgen receptor antagonist (-)-arabilin: a strategic, biomimetic [1,7]-hydrogen shift Isolation and structure elucidation of a novel androgen antagonist, arabilin, produced by Streptomyces sp. MK756-CF1. Asymmetric induction in 8π electrocyclizations. Design of a removable chiral auxiliary
is cites work of	wds:Q37484247-84FC4711-DAC1-4621-AB5D-D6CEA8AA9B66 wds:Q33625206-FC173A6D-F412-40D8-B7DB-B0712DFC197C wds:Q35872273-0528E95A-EDBB-40B8-9F53-4E91CCFB8B7B wds:Q39663649-203FAAE5-8F5E-4E85-9FE6-9980CA95BAB1 wds:Q61774206-F2727B4A-3D5D-480A-AA5A-8A220120FA8A wds:Q35872290-300CCE02-A59B-4069-9EF3-373F955D77EB

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