Stereocontrolled Synthesis of Adjacent Acyclic Quaternary-Tertiary Motifs: Application to a Concise Total Synthesis of (-)-Filiformin

被引:38
作者
Blair, Daniel J. [1 ]
Fletcher, Catherine J. [1 ]
Wheelhouse, Katherine M. P. [2 ]
Aggarwal, Varinder K. [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[2] GlaxoSmithKline UK LtD, Stevenage SG1 2NY, Herts, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
boron; enantioselectivity; lithium; natural products; total synthesis; BORONIC ESTERS; ENANTIOSELECTIVE CONSTRUCTION; STEREOSELECTIVE CONSTRUCTION; SECONDARY ALCOHOLS; HOMOLOGATION; BORYLATION; CONVERSION; REARRANGEMENT; GENERATION; BORANES;
D O I
10.1002/anie.201400944
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithiation/borylation methodology has been developed for the synthesis of acyclic quaternary-tertiary motifs with full control of relative and absolute stereochemistry, thus leading to all four possible isomers of a stereodiad. A novel intramolecular Zweifel-type olefination enabled acyclic stereocontrol to be transformed into cyclic stereocontrol. These key steps have been applied to the shortest enantioselective synthesis of (-)-filiformin to date (9 steps) with full stereocontrol.
引用
收藏
页码:5552 / 5555
页数:4
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