Chiral synthesis of polyketide-derived natural products. XXXIV. Facile total synthesis of carbonolides by Witting-Horner macro-cyclization and stereoselective expoxidation.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/39/1/39_1_64/_pdf
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Catalytic multicomponent reaction involving a ketyl-type radical;Nature Synthesis;2022-06-13
2. Computational study on formation of 15-membered azalactone by double reductive amination using molecular mechanics and density functional theory calculations;The Journal of Antibiotics;2018-03-07
3. ChemInform Abstract: Chiral Synthesis of Polyketide-Derived Natural Products. Part 34. Facile Total Synthesis of Carbonolides by Wittig-Horner Macrocyclization and Stereoselective Epoxidation.;ChemInform;2010-08-22
4. Synthesis of the Cyclobutylfuran Sector of Providencin via Zirconium-mediated Oxygen Abstraction from a Furanoside;Organic Letters;2009-02-25
5. Total synthesis of an aglycone of spiramycin;Tetrahedron Letters;1998-03
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