A Stereoselective Formal Synthesis of (−)‐Fumagillol
- 30 August 2004
- journal article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2004 (18), 3813-3819
- https://doi.org/10.1002/ejoc.200400262
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Total Synthesis of (−)‐Spirotryprostatin BAngewandte Chemie International Edition, 2003
- Concise stereocontrolled routes to fumagillol, fumagillin, and TNP-470Chirality, 2003
- Progress in fumagillin synthesisPublished by Walter de Gruyter GmbH ,2003
- Design and synthesis of highly potent fumagillin analogues from homology modeling for a human MetAP-2Bioorganic & Medicinal Chemistry Letters, 2000
- Synthesis and Absolute Stereochemical Assignment of (+)-MiyakolideJournal of the American Chemical Society, 1999
- Synthesis of (−)-FumagillinJournal of the American Chemical Society, 1999
- Synthesis of (−)-malyngolide using reactions of alkylidenecarbenesJournal of the Chemical Society, Perkin Transactions 1, 1998
- Chemical Modification of Fumagillin. III. Modification of the Spiro-epoxide.CHEMICAL & PHARMACEUTICAL BULLETIN, 1995
- Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growthNature, 1990
- Isolierung und Strukturaufklärung von OvalicinHelvetica Chimica Acta, 1968