Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/16388
Title: Enantioselective total synthesis of natural 11,12-epoxycembrene-C
Authors: Li, YL
Liu, ZS
Lan, J
Li, J
Peng, LZ
Li, WZ
Li, Y
Chan, ASC
Keywords: Cembrane diterpenoid
McMurry coupling
Sharpless epoxidation
11,12-epoxycembrene-C
Total synthesis
Issue Date: 2000
Publisher: Pergamon-Elsevier Science Ltd
Source: Tetrahedron letters, 2000, v. 41, no. 39, p. 7465-7469 How to cite?
Journal: Tetrahedron Letters 
Abstract: The first enantioselective total synthesis of (+)-11,12-epoxycembrene-C (1), a novel naturally occurring cembranoxide isolated from tropical marine soft coral, was achieved via a general approach by employing an intramolecular McMurry coupling and Sharpless asymmetric epoxidation as key steps from readily available starting materials.
URI: http://hdl.handle.net/10397/16388
ISSN: 0040-4039
DOI: 10.1016/S0040-4039(00)00982-5
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