70117-00-9Relevant articles and documents
Synthetic Studies on Enantioselective Total Synthesis of Cyathane Diterpenoids: Cyrneines A and B, Glaucopine C, and (+)-Allocyathin B2
Wu, Guo-Jie,Zhang, Yuan-He,Tan, Dong-Xing,He, Long,Cao, Bao-Chen,He, Yu-Peng,Han, Fu-She
, (2019/03/19)
The details for the synthetic studies on enantioselective total synthesis of cyathane diterpenoids cyrneine A (1) and B (2), glaucopine C (3), and (+)-allocyathin B2 are presented. We established a mild Suzuki coupling for heavily substituted n
Total synthesis of (+)-allocyathin B2
Trost, Barry M.,Dong, Li,Schroeder, Gretchen M.
, p. 2844 - 2845 (2007/10/03)
The first enantioselective synthesis of (+)-allocyathin was achieved. The synthesis features a Pd-catalyzed asymmetric allylic alkylation to install the first quaternary center, a Ru-catalyzed diastereoselective cycloisomerization to construct the six-mem
Metabolites of bird's nest fungi. Part II. Diterpenoid metabolites of Cyathus earlei Lloyd
Ayer,Lee
, p. 3332 - 3337 (2007/10/10)
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