4.8 Article

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

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 22, 页码 5552-5555

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201400944

关键词

boron; enantioselectivity; lithium; natural products; total synthesis

资金

  1. EPSRC
  2. GSK
  3. European Research Council (FP7, ERC grant) [246785]
  4. European Research Council (ERC) [246785] Funding Source: European Research Council (ERC)
  5. Engineering and Physical Sciences Research Council [EP/I038071/1] Funding Source: researchfish
  6. EPSRC [EP/I038071/1] Funding Source: UKRI

向作者/读者索取更多资源

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.

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