4.8 Article

Enantioselective construction of quaternary carbon centers by catalytic [2+2+2] cycloaddition of 1,6-enynes and alkynes

Journal

ORGANIC LETTERS
Volume 7, Issue 22, Pages 4955-4957

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol051876j

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[GRAPHICS] The enantioselective [2 + 2 + 2] cycloaddition of 1,6-enynes and alkynes using chiral rhodium catalysts gave cycloadducts containing quaternary carbon stereocenters. Both symmetrical and unsymmetrical alkynes and acetylene could be used as coupling partners, and the corresponding bicyclic cyclohexa-1,3-dienes were obtained in good to excellent ee.

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