An Improved Asymmetric Synthesis of Malyngamide U and Its 2′-Epimer-Reference-Cited by-同舟云学术

An Improved Asymmetric Synthesis of Malyngamide U and Its 2′-Epimer

Published:2008-07-26 Issue:17 Volume:73 Page:6873-6876
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Feng Jian-Peng¹,Shi Zi-Fa¹,Li Yang¹,Zhang Jun-Tao¹,Qi Xian-Liang¹,Chen Jie¹,Cao Xiao-Ping¹

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo800876u

Reference36 articles.

1. Hermitamides A and B, Toxic Malyngamide-Type Natural Products from the Marine Cyanobacterium Lyngbya majuscula

2. Three New Malyngamides from a Papua New Guinea Collection of the Marine Cyanobacterium Lyngbya majuscula

3. Brief overview of the family of the related malyngamides. For the most recent and, see refand references cited therein.

4. Malyngamide X: The First (7R)-Lyngbic Acid that Connects to a New Tripeptide Backbone from the Thai Sea HareBursatella leachii

5. Total synthesis of malyngamide X and its 7′S-epi isomer

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