Trost Barry M, Yang Hanbiao, Thiel Oliver R, Frontier Alison J, Brindle Cheyenne S
Department of Chemistry, Stanford University, Stanford, California 94305, USA.
J Am Chem Soc. 2007 Feb 28;129(8):2206-7. doi: 10.1021/ja067305j. Epub 2007 Feb 6.
A ring expanded bryostatin analogue was synthesized by utilizing a Ru-catalyzed tandem tetrahydropyran formation, a Pd-catalyzed tandem dihydropyran formation, and a ring-closing metathesis (RCM) as key steps. The analogue possesses potent anti-tumor activity against the NCI-ADR cancer cell line with an IC of 123 nM.
通过将钌催化的串联四氢吡喃形成、钯催化的串联二氢吡喃形成以及关环复分解反应（RCM）作为关键步骤，合成了一种环扩展的苔藓抑素类似物。该类似物对NCI-ADR癌细胞系具有强大的抗肿瘤活性，IC50为123 nM。
