Catalytic enantioselective silylation of acyclic and cyclic triols: application to total syntheses of cleroindicins D, F, and C
Z You, AH Hoveyda, ML Snapper
Index: You, Zhen; Hoveyda, Amir H.; Snapper, Marc L. Angewandte Chemie - International Edition, 2009 , vol. 48, # 3 p. 547 - 550
Full Text: HTML
Citation Number: 58
Abstract
Catalysts that promote site-selective modification of polyfunctional molecules can be of significant utility in selective chemical synthesis.[1] Of particular importance are chiral catalysts that initiate enantioselective functionalization of polyoxygenated molecules [2]— entities commonly found among biologically active agents. Herein, we present methods for the enantioselective silylations [3] of acyclic and cyclic 1, 2, 3-triols [Eq.(1)]; the ...
Related Articles:
First synthesis of (+)-rengyolone and (+)-and (−)-menisdaurilide
[Canto, Mariona; De March, Pedro; Figueredo, Marta; Font, Josep; Rodriguez, Sonia; Alvarez-Larena, Angel; Piniella, Juan F. Tetrahedron Asymmetry, 2002 , vol. 13, # 5 p. 455 - 459]