About: Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents

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About: Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2000 (uk) im Oktober 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2000 (ast) scientific article published on 01 October 2000 (en)
publication date	wds:Q73014855-F1C2EEDE-2343-453F-81B3-7DCA3DF36896
publication date	2000-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73014855-1CC88BC2-DD3C-4898-B848-3E338347EB50 wds:Q73014855-24DEEC23-570C-4A4F-A490-738466EC9AD8 wds:Q73014855-301F2394-9884-4B6E-A147-34BCE4267DF5 wds:Q73014855-B379C549-7F3C-44C3-AF3C-AB9A151D7EC6
author name string	F Compernolle T De Wit G J Hoornaert K Van Emelen
rdfs:label	Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (en) Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (nl)
skos:prefLabel	Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (en) Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (nl)
name	Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (en) Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (nl)
title	wds:Q73014855-009A8D24-B589-43B1-916E-0FCDB69A7D06
title	Diastereoselective intramolecular Ritter reaction: generation of a cis-fused hexahydro-4aH-indeno[1,2-b]pyridine ring system with 4a,9b-diangular substituents (en)
page(s)	wds:Q73014855-209180C8-9FF3-4AFD-9997-0A58D3682183
page(s)	3083-3086
instance of	wds:Q73014855-C92BCB13-38AA-44BA-B039-A3170483FC2D
instance of	scholarly article
PubMed ID	wds:Q73014855-A7D65C5A-A90C-4E88-9027-DCD203020E91
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11009351
PubMed ID	11009351
published in	wds:Q73014855-C861ABFF-42AB-46D8-87EE-AD789782B527
published in	Organic Letters
issue	wds:Q73014855-FCD406D7-FABE-4D73-B193-F7E66DA2353F
volume	wds:Q73014855-F08D7626-221B-480D-8957-54AA7307DBC3
issue	20
volume	2
DOI	wds:Q73014855-E8C8A37D-540A-4E2D-913C-0CB71DC25F66
DOI	http://dx.doi.org/10.1021/OL006248A
DOI	10.1021/OL006248A
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73014855
is cites work of	A Direct and Stereoretentive Synthesis of Amides from Cyclic Alcohols Stereoretentive Copper (II) Catalyzed Ritter Reactions of Secondary Cycloalkanols A novel, tandem construction of C-N and C-C bonds: facile and one-pot transformation of the Baylis-Hillman adducts into 2-benzazepines
is cites work of	wds:Q37412410-DAFDC0DA-7D83-4581-8F80-4AAF87E085B0 wds:Q37329150-7FBC4729-C7BD-4E48-8B1C-F4A264CD99F8 wds:Q44737607-B0A6C0B4-898B-4FA3-B576-13BBB841CDF5

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