ChemInform Abstract: Highly Enantioselective Synthesis of Chiral Pyranonaphthoquinone‐Fused Spirooxindoles Through Organocatalytic Three‐Component Cascade Reactions. Issue 37 (September 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Highly Enantioselective Synthesis of Chiral Pyranonaphthoquinone‐Fused Spirooxindoles Through Organocatalytic Three‐Component Cascade Reactions. Issue 37 (September 2015)
Main Title:: ChemInform Abstract: Highly Enantioselective Synthesis of Chiral Pyranonaphthoquinone‐Fused Spirooxindoles Through Organocatalytic Three‐Component Cascade Reactions.
Authors:: Zhao, Hong‐Wu
Li, Bo
Tian, Ting
Meng, Wei
Yang, Zhao
Song, Xiu‐Qing
Chen, Xiao‐Qin
Pang, Hai‐Liang
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In the presence of cinchona‐thiourea organocatalyst, the enantioselective three‐component cascade reaction of isatins, malononitrile, and 2‐hydroxynaphthalene‐1, 4‐diones proceeds readily to furnish chiral pyranonaphthoquinone‐fused spirooxindoles.</p> </abstract>
Is Part Of:: ChemInform. Volume 46:Issue 37(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 37(2015)
Issue Display:: Volume 46, Issue 37 (2015)
Year:: 2015
Volume:: 46
Issue:: 37
Issue Sort Value:: 2015-0046-0037-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-09
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.201537123 ↗
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:: 3505.xml