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Highly diastereo- and enantioselective CuH-catalyzed synthesis of 2,3-disubstituted indolines.

ABSTRACT: A diastereo- and enantioselective CuH-catalyzed method for the preparation of highly functionalized indolines is reported. The mild reaction conditions and high degree of functional group compatibility as demonstrated with substrates bearing heterocycles, olefins, and substituted aromatic groups, renders this technique highly valuable for the synthesis of a variety of cis-2,3-disubstituted indolines in high yield and enantioeselectivity.

SUBMITTER: Ascic E

PROVIDER: S-EPMC4440622 | biostudies-literature | 2015 Apr

REPOSITORIES: biostudies-literature

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Highly diastereo- and enantioselective CuH-catalyzed synthesis of 2,3-disubstituted indolines.

Ascic Erhad E Buchwald Stephen L SL

Journal of the American Chemical Society 20150406 14

A diastereo- and enantioselective CuH-catalyzed method for the preparation of highly functionalized indolines is reported. The mild reaction conditions and high degree of functional group compatibility as demonstrated with substrates bearing heterocycles, olefins, and substituted aromatic groups, renders this technique highly valuable for the synthesis of a variety of cis-2,3-disubstituted indolines in high yield and enantioeselectivity. ...[more]

PMID: 25826004

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