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Chiral Phosphine Lewis Bases Catalyzed Asymmetric aza-Baylis−Hillman Reaction of N-Sulfonated Imines with Activated Olefins

✍ Scribed by Shi, Min; Chen, Lian-Hui; Li, Chao-Qun

Book ID: 126883310
Publisher: American Chemical Society
Year: 2005
Tongue: English
Weight: 272 KB
Volume: 127
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja0447255

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Chiral Phosphine Lewis Bases Catalyzed A

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Dendritic Chiral Phosphine Lewis Bases-C

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## Abstract A series of polyether dendritic chiral phosphine Lewis bases was synthesized, and successfully applied to the asymmetric aza‐Morita–Baylis–Hillman reaction of __N__‐sulfonated imines (__N__‐arylmethylidene‐4‐methylbenzenesulfonamides) with methyl vinyl ketone (MVK), ethyl vinyl ketone (

ChemInform Abstract: Dendritic Chiral Ph

ChemInform Abstract: Dendritic Chiral Phosphine Lewis Bases-Catalyzed Asymmetric Aza-Morita—Baylis—Hillman Reaction of N-Sulfonated Imines with Activated Olefins.

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Asymmetric Aza-Morita—Baylis—Hillman Rea

Asymmetric Aza-Morita—Baylis—Hillman Reaction of N-Sulfonated Imines with Activated Olefins Catalyzed by Chiral Phosphine Lewis Bases Bearing Multiple Phenol Groups.

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Chiral Phosphine Lewis Base Catalyzed As

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.