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Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization.

ABSTRACT: Functionalized 4- and 6-azaindolines are accessible with high levels of enantioselectivity by the cation-directed cyclization of aminopyridine-derived imines via phase-transfer catalysis. The extension of this methodology to diastereoselective cyclizations is also described.

SUBMITTER: Lamb AD

PROVIDER: S-EPMC5086784 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description: Not available

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