4.7 Article

Asymmetric total synthesis of (+)-fumimycin via 1,2-addition to ketimines

Journal

CHEMICAL COMMUNICATIONS
Volume 46, Issue 48, Pages 9215-9217

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc03399e

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Funding

  1. German Business Foundation
  2. NSF [CHE-0840513]

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The first asymmetric total synthesis of fumimycin was accomplished. As a key step, a 1,2-addition of methyl Grignard reagents to ketimines with quinine as additive was employed. The absolute configuration of (+)-fumimycin was determined by CD-spectroscopy combined with time-dependent density functional calculations.

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