Iterative Direct Aldol Strategy for Polypropionates: Enantioselective Total Synthesis of (−)-Membrenone A and B
Author:
Affiliation:
1. Institute of Microbial Chemistry (BIKAKEN), Tokyo, 3-14-23 Kamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan
2. JST, ACT-C, 3-14-23 Kamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan
Funder
Japan Society for the Promotion of Science
Japan Science and Technology Agency
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol5024932
Reference48 articles.
1. Membrenones : New polypropionates from the skin of the mediterranean mollusc Pleurobranchus membranaceus
2. Stereoselective synthesis of an isomer of Membrenone-C via an aldol based two directional chain extension
3. Stereoselective Synthesis of Dihydropyrone-Containing Marine Natural Products. Total Synthesis and Structural Elucidation of (−)-Membrenone-C
4. Total Synthesis of (−)-(6S,7S,8S,9R,10S,2‘S)-Membrenone-A and (−)-(6S,7S,8S,9R,10S)- Membrenone-B and Structural Assignment of Membrenone-C
5. Total Synthesis of (−)- and (+)-Membrenone C
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