Asymmetric Aldol Reaction of Acetaldehyde and Isatin Derivatives for the Total Syntheses of ent-Convolutamydine E and CPC-1 and a Half Fragment of Madindoline A and B-Reference-Cited by-同舟云学术

Asymmetric Aldol Reaction of Acetaldehyde and Isatin Derivatives for the Total Syntheses of ent-Convolutamydine E and CPC-1 and a Half Fragment of Madindoline A and B

Published:2009-08-05 Issue:17 Volume:11 Page:3854-3857
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Itoh Takahiko¹,Ishikawa Hayato¹,Hayashi Yujiro¹

Affiliation:

1. Department of Industrial Chemistry, Faculty of Engineering, and Research Institute for Science and Technology, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol901432a

Reference49 articles.

1. Convolutamydine A, a novel bioactive hydroxyoxindole alkaloid from marine bryozoan Amathia convoluta

2. Isolation and structure of convolutamydines B ∼ D from marine bryozoan Amathia convoluta

3. Three New Alkaloids, Convolutamines F and G, and Convolutamydine E, from the Floridian Marine Bryozoan Amathia convoluta

4. Madindoline, a Novel Inhibitor of IL-6 Activity from Streptomyces sp. K93-0711. I. Taxonomy, Fermentation, Isolation and Biological Activities.

5. Madindolines, Novel Inhibitors of IL-6 Activity from Streptomyces sp. K93-0711. II. Physico-chemical Properties and Structural Elucidation.

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