83159-26-6Relevant articles and documents
Asymmetric Total Syntheses of 8,9-Seco-ent-kaurane Diterpenoids Enabled by an Electrochemical ODI-[5+2] Cascade
Ding, Hanfeng,Gao, Beiling,Liu, Zhaobo,Tong, Zhenzhong,Wang, Bingnan
supporting information, p. 14892 - 14896 (2021/06/08)
An electrochemical ODI-[5+2] cascade reaction was developed which enables the rapid assembly of diversely functionalized bicyclo[3.2.1]octadienones from sensitive ethynylphenols. By combining a directed retro-aldol/aldol process, a [2,3]-sigmatropic rearr
Direct asymmetric entry into the cytotoxic 8,9-secokaurene diterpenoids. Total synthesis of (-)-O-methylshikoccin and (+)-O-(methylepoxy)shikoccin
Paquette, Leo A.,Backhaus, Dirk,Braun, Ralf
, p. 11990 - 11991 (2007/10/03)
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Three new 8,9-seco-ent-kaurane diterpenoids from Rabdosia shikokiana (Labiatae)
Node,Ito,Fuji,Fujita
, p. 2639 - 2640 (2007/10/02)
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