Second-generation total synthesis of (-)-diversifolin

被引:8
|
作者
Tsuboi, Kazuma [1 ]
Nakamura, Tomoaki [1 ]
Suzuki, Takahiro [1 ]
Nakazaki, Atsuo [1 ]
Kobayashi, Susumu [1 ]
机构
[1] Tokyo Univ Sci RIKADAI, Fac Pharmaceut Sci, Noda, Chiba 2788510, Japan
基金
日本学术振兴会;
关键词
NF-KAPPA-B; RING-CLOSING METATHESIS; SESQUITERPENE LACTONES; OLEFIN METATHESIS; ALDEHYDES; INHIBITION; COMPLEXES; LIGANDS; ETHERS; ESTERS;
D O I
10.1016/j.tetlet.2010.02.012
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A second-generation total synthesis of (-)-diversifolin has been achieved by a more straightforward strategy. involving a highly stereochemistry-dependent 10-membered ring-closing metathesis and a stereoselective dihydroxylation/lactone transposition sequence. Compared to Our previous synthesis, the present synthesis is improved in the yield of the key intermediate 2 (20% in 12 steps from diol 8). (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1876 / 1879
页数:4
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