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Protecting-Group-Free Total Synthesis of (-)-Boscartin A in 3 Steps from (-)-Boscartin F via Wharton Reaction
被引:1
|作者:
Kamo, Shogo
[1
]
Kasamatsu, Akihiko
[1
]
Shiraiwa, Junya
[1
]
Matsuzawa, Akinobu
[1
]
Sugita, Kazuyuki
[1
]
机构:
[1] Hoshi Univ, Dept Synthet Med Chem, Fac Pharmaceut Sci, 2-4-41 Ebara,Shinagawa Ku, Tokyo 1428501, Japan
关键词:
boscartin A;
enantioselective;
protecting-group-free;
total synthesis;
Wharton reaction;
SOFT;
CEMBRANOIDS;
STEREOCHEMISTRY;
DITERPENOIDS;
RESIN;
D O I:
10.1002/ejoc.202201366
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
In this report, we described the first total synthesis of (-)-boscartin A, a cembranoid featuring a 5/5/12-fused tricyclic structure. Via the key reactions, including stereoselective epoxidation and Wharton reaction, (-)-Boscartin A was obtained in three steps from (-)-boscartin F, with 46 % overall yield.
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