Expeditious synthesis of highly substituted indolizinones via a palladium-catalyzed domino sequence

Ikyon Kim; Kyungsun Kim

doi:10.1021/ol1006778

Expeditious synthesis of highly substituted indolizinones via a palladium-catalyzed domino sequence

Ikyon Kim, Kyungsun Kim

Department of Pharmacy

Research output: Contribution to journal › Article › peer-review

44 Citations (Scopus)

Abstract

A direct one-pot approach to polysubstituted indolizinones from tertiary propargylic alcohols using a palladium-catalyzed domino process involving aminopalladation, reductive elimination, and 1,2-shift is described.

Original language	English
Pages (from-to)	2500-2503
Number of pages	4
Journal	Organic Letters
Volume	12
Issue number	11
DOIs	https://doi.org/10.1021/ol1006778
Publication status	Published - 2010 Jun 4

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol1006778

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title = "Expeditious synthesis of highly substituted indolizinones via a palladium-catalyzed domino sequence",

abstract = "A direct one-pot approach to polysubstituted indolizinones from tertiary propargylic alcohols using a palladium-catalyzed domino process involving aminopalladation, reductive elimination, and 1,2-shift is described.",

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AU - Kim, Kyungsun

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N2 - A direct one-pot approach to polysubstituted indolizinones from tertiary propargylic alcohols using a palladium-catalyzed domino process involving aminopalladation, reductive elimination, and 1,2-shift is described.

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Expeditious synthesis of highly substituted indolizinones via a palladium-catalyzed domino sequence

Abstract

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