Enantioselective total synthesis of natural 11,12-epoxycembrene-C
摘要:
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. (C) 2000 Elsevier Science Ltd. All rights reserved.
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. (C) 2000 Elsevier Science Ltd. All rights reserved.
Bowden, Bruce F.; Coll, John C.; Tapiolas, Dianne M., Australian Journal of Chemistry, 1983, vol. 36, # 11, p. 2289 - 2296
作者:Bowden, Bruce F.、Coll, John C.、Tapiolas, Dianne M.