Enantioselective Total Synthesis of Chondrosterins I and J by Catalytic Asymmetric Intramolecular Aldol Reaction Using Chiral Diamine Catalyst
Author:
Affiliation:
1. School of Life Sciences; Tokyo University of Pharmacy and Life Sciences; 1432-1 Horinouchi, Hachioji 192-0392 Tokyo Japan
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.202000579/fullpdf
Reference74 articles.
1. Induced Marine Fungus Chondrostereum sp. as a Means of Producing New Sesquiterpenoids Chondrosterins I and J by Using Glycerol as the Carbon Source
2. Isolation and Structural Elucidation of Chondrosterins F–H from the Marine Fungus Chondrostereum sp.
3. Chondrosterins A–E, Triquinane-Type Sesquiterpenoids from Soft Coral-Associated Fungus Chondrostereum sp.
4. Hirsutane Sesquiterpenoids from the Marine-Derived Fungus Chondrostereum sp.
5. Total synthesis of (±)-chondrosterin I using a desymmetric aldol reaction
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