150930-60-2Relevant academic research and scientific papers
Total synthesis of the cembranoid diterpene lactone (+)-cleomeolide. Some remarkable conformational features of nine-membered belts linked in 2,6-fashion to a methylenecyclohexane core
Paquette, Leo A.,Wang, Ting-Zhong,Philippo, Christophe M. G.,Wang, Shaopeng
, p. 3367 - 3374 (1994)
The total synthesis of (+)-cleomeolide (1) has been accomplished. The key construction elements of this cembranoid lactone were (i) improved conversion of optically pure Wieland-Miescher ketone into dienol ether 12 and oxidative cleavage of the latter to
Enantioselective synthesis of (+)-cleomeolide, the structurally unique diterpene lactone constituent of Cleome viscosa
Paquette,Wang,Wang,Philippo
, p. 3523 - 3526 (2007/10/02)
The first total synthesis of (+)-cleomeolide has been accomplished in enantioselective fashion from optically pure Wieland-Miescher ketone.
