ChemInform Abstract: Unified Approach to the Spiro(pyrrolidinyl‐oxindole) and Hexahydropyrrolo[2, 3‐b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A. Issue 17 (April 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Unified Approach to the Spiro(pyrrolidinyl‐oxindole) and Hexahydropyrrolo[2, 3‐b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A. Issue 17 (April 2016)
Main Title:: ChemInform Abstract: Unified Approach to the Spiro(pyrrolidinyl‐oxindole) and Hexahydropyrrolo[2, 3‐b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A.
Authors:: De, Subhadip
Das, Mrinal Kanti
Bhunia, Subhajit
Bisai, Alakesh
Abstract:: Abstract: An enantioselective 3‐hydroxymethylation of 3‐substituted oxindoles is described.
Is Part Of:: ChemInform. Volume 47:Issue 17(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 17(2016)
Issue Display:: Volume 47, Issue 17 (2016)
Year:: 2016
Volume:: 47
Issue:: 17
Issue Sort Value:: 2016-0047-0017-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-04
Subjects:: indole derivatives, isoindole derivatives -- fused pyrrole derivatives -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- organocatalysis
Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chin.201617121 ↗
Languages:: English
ISSNs:: 0931-7597
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 25.xml