4.8 Article

Single-Pot Asymmetric Approach toward Enantioenriched Quaternary Stereocenter-Containing Alkylidenecyclobutanes

Journal

ORGANIC LETTERS
Volume 18, Issue 12, Pages 3022-3025

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01432

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Funding

  1. Chemical Industry Fund (FCI Liebig-fellowship) through Liebig-Stipendium

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Enantioenriched alkylidenecyclobutanes possessing a quaternary stereogenic center, usually difficult to access, have been synthesized by combining a double boron-homologation and an allylboration through a highly efficient and diastereoselective one-pot process. Starting from commercially available substrates, this protocol represents a simple way of accessing chiral unsaturated four-membered ring systems with excellent stereoisomeric ratios.

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