ChemInform Abstract: Enantioselective Steglich Rearrangement of Oxindole Derivatives by Easily Accessible Chiral N, N‐4‐(Dimethylamino)pyridine Derivatives. Issue 5 (January 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Enantioselective Steglich Rearrangement of Oxindole Derivatives by Easily Accessible Chiral N, N‐4‐(Dimethylamino)pyridine Derivatives. Issue 5 (January 2016)
Main Title:: ChemInform Abstract: Enantioselective Steglich Rearrangement of Oxindole Derivatives by Easily Accessible Chiral N, N‐4‐(Dimethylamino)pyridine Derivatives.
Authors:: Mandai, Hiroki
Fujiwara, Takuma
Noda, Katsuaki
Fujii, Kazuki
Mitsudo, Koichi
Korenaga, Toshinobu
Suga, Seiji
Abstract:: Abstract: The rearrangement of O‐acylated oxidoles proceeds smoothly in the presence of chiral pyridine catalysts (I) to give oxindole derivatives in excellent yields with enantioselectivities up to 98%.
Is Part Of:: ChemInform. Volume 47:Issue 5(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 5(2016)
Issue Display:: Volume 47, Issue 5 (2016)
Year:: 2016
Volume:: 47
Issue:: 5
Issue Sort Value:: 2016-0047-0005-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-01
Subjects:: indole derivatives, isoindole derivatives -- rearrangements -- 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.201605134 ↗
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:: 682.xml