4.8 Article

Nickel-Catalyzed Reductive Vinylation of Chloro-hexahydropyrroloindoline Derivatives with Vinyl Triflates

Journal

ORGANIC LETTERS
Volume 23, Issue 7, Pages 2493-2497

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c00431

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Funding

  1. National Natural Science Foundation of China [21871173]

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This study demonstrates a facile method for constructing C-3a vinyl substituted hexahydropyrrolidinoindolines based on Ni-catalyzed reductive coupling, showcasing remarkable compatibility with a wide range of alkyl-decorated vinyl triflates, including sterically hindered branched vinyl groups.
This work emphasizes facile construction of C-3a vinyl substituted hexahydropyrrolidinoindolines based upon Ni-catalyzed reductive coupling of chloro-hexahydropyrroloindoline derivatives with a wide range of alkyl-decorated vinyl triflates. The remarkable compatibility of sterically hindered branched vinyl groups is highlighted.

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