Asymmetric Synthesis of 2-Alkyl-Substituted 2,5-Dihydropyrroles from Optically Active Aza-Baylis−Hillman Adducts. Formal Synthesis of (−)-Trachelanthamidine.-Reference-Cited by-同舟云学术

Asymmetric Synthesis of 2-Alkyl-Substituted 2,5-Dihydropyrroles from Optically Active Aza-Baylis−Hillman Adducts. Formal Synthesis of (−)-Trachelanthamidine.

Published:2010-05-13 Issue:11 Volume:75 Page:3578-3586
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ishikawa Shingo¹,Noguchi Fumiaki¹,Kamimura Akio¹

Affiliation:

1. Department of Applied Molecular Bioscience, Graduate School of Medicine, Yamaguchi University, Ube 755-8611, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo100315j

Reference87 articles.

1. Aza‐Baylis–Hillman Reactions and Their Synthetic Applications

2. aza-Baylis−Hillman Reaction

3. Novel Asymmetric C−C Bond Formation Process Promoted by Et2AlCl and Its Application to the Stereoselective Synthesis of Unusual β-Branched Baylis−Hillman Adducts

4. Catalytic, Asymmetric Baylis–Hillman Reaction of Imines with Methyl Vinyl Ketone and Methyl Acrylate

5. Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis–Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate

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