ChemInform Abstract: Stereoselective Synthesis of 1‐Methyl‐3′, 4′, 5′, 6′‐tetrahydrospiro[indoline‐3, 2′‐pyran]‐2‐one Derivatives via Prins Cyclization. Issue 41 (October 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Stereoselective Synthesis of 1‐Methyl‐3′, 4′, 5′, 6′‐tetrahydrospiro[indoline‐3, 2′‐pyran]‐2‐one Derivatives via Prins Cyclization. Issue 41 (October 2015)
Main Title:: ChemInform Abstract: Stereoselective Synthesis of 1‐Methyl‐3′, 4′, 5′, 6′‐tetrahydrospiro[indoline‐3, 2′‐pyran]‐2‐one Derivatives via Prins Cyclization.
Authors:: Damera, Krishna
Yu, Bingchen
Wang, Binghe
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Spirooxindole alcohols (III) and fluorides (IV) are readily prepared as single diastereomers by a Lewis acid promoted Prins cyclization of 3‐allyl‐3‐hydroxy indolinones (I) with aldehydes (II).</p> </abstract>
Is Part Of:: ChemInform. Volume 46:Issue 41(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 41(2015)
Issue Display:: Volume 46, Issue 41 (2015)
Year:: 2015
Volume:: 46
Issue:: 41
Issue Sort Value:: 2015-0046-0041-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-10
Subjects:: 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.201541115 ↗
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:: 2984.xml