Enantioselective Biomimetic Total Syntheses of Katsumadain and Katsumadain C-Reference-Cited by-同舟云学术

Enantioselective Biomimetic Total Syntheses of Katsumadain and Katsumadain C

Published:2011-12-13 Issue:1 Volume:14 Page:162-165
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Pengtao¹,Wang Yongguang¹,Bao Ruiyang¹,Luo Tuoping¹,Yang Zhen¹,Tang Yefeng¹

Affiliation:

1. The Comprehensive AIDS Research Center, Department of Pharmacology & Pharmaceutical Sciences, School of Medicine, Tsinghua University, Beijing 100084, China, and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education and Beijing National Laboratory for Molecular Science (BNLMS), College of Chemistry, Peking University, Beijing 100871, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2029433

Reference27 articles.

1. 2-Pyrone natural products and mimetics: isolation, characterisation and biological activity

2. Natural and synthetic 2H-pyran-2-ones and their versatility in organic synthesis

3. A [2 + 2] Cycloaddition Dimer and a Diels–Alder Adduct fromAlpinia katsumadai

4. New Diarylheptanoids and Kavalactone fromAlpinia katsumadaiHayata

5. Rapid Biomimetic Total Synthesis of (±)-Rossinone B

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