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Pd(0)-Catalyzed [1,5]-Sigmatropic Hydrogen Shift of Propargylic Esters toward Substituent Naphthylamines

Year: 2011

Type: article

Abstract: A novel and convenient carboannulation method for the synthesis of highly substituted naphthylamine derivatives has been developed though a Pd(0)-catalyzed [1,5]-sigmatropic hydrogen shift and cyclization reaction of propargyl esters.

Source: The Journal of Organic Chemistry

DOI: 10.1021/jo1024267

Authors: Shu-Chun Zhao, Xing-Zhong Shu, Ke-Gong Ji, An-Xi Zhou, Ting He, Xue-Yuan Liu, Yong-Min Liang

Institutions: State Key Laboratory of Applied Organic Chemistry, Lanzhou University

Language: English

Topic: Catalytic Alkyne Reactions

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: green

Funders: National Science Foundation, National Key Research and Development Program of China

OpenAlex ID: W1978188231

FWCI: 3.052

Cites: 49

Cited by: 39

Related to: 10