ChemInform Abstract: Synthesis of Spiro[chroman/tetrahydrothiophene‐3, 3′‐oxindole] Scaffolds via Heteroatom‐Michael—Michael Reactions: Easily Controlled Enantioselectivity via Bifunctional Catalysts. Issue 33 (19th August 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: Synthesis of Spiro[chroman/tetrahydrothiophene‐3, 3′‐oxindole] Scaffolds via Heteroatom‐Michael—Michael Reactions: Easily Controlled Enantioselectivity via Bifunctional Catalysts. Issue 33 (19th August 2014)
Main Title:: ChemInform Abstract: Synthesis of Spiro[chroman/tetrahydrothiophene‐3, 3′‐oxindole] Scaffolds via Heteroatom‐Michael—Michael Reactions: Easily Controlled Enantioselectivity via Bifunctional Catalysts.
Authors:: Huang, Youming
Zheng, Changwu
Chai, Zhuo
Zhao, Gang
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Stereodefined spirooxindoles are prepared via thiourea‐catalyzed Michael‐Michael‐reaction.</p> </abstract>
Is Part Of:: ChemInform. Volume 45:Issue 33(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 33(2014)
Issue Display:: Volume 45, Issue 33 (2014)
Year:: 2014
Volume:: 45
Issue:: 33
Issue Sort Value:: 2014-0045-0033-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-08-19
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.201433117 ↗
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:: 3340.xml