Indium-mediated tandem dimerization and cyclization of nitrqones and aldimines to 3-arylaminodihydrobenzofurans under aqueous conditions

Arumugasamy Jeevanandam; Yong-Chien Ling

doi:10.1016/S0040-4039(01)00655-4

Back

Indium-mediated tandem dimerization and cyclization of nitrqones and aldimines to 3-arylaminodihydrobenzofurans under aqueous conditions

Journal article

Peer reviewed

Indium-mediated tandem dimerization and cyclization of nitrqones and aldimines to 3-arylaminodihydrobenzofurans under aqueous conditions

Arumugasamy Jeevanandam and Yong-Chien Ling

Tetrahedron Letters, Vol.42(26), pp.4361-4362

25/06/2001

DOI: https://doi.org/10.1016/S0040-4039(01)00655-4

Abstract

Deoxygenative reductive coupling

Diastereomers

Tandem dimerization and cyclization

Vicinal diamines

Nitrones undergo deoxygenative reductive coupling and subsequent cyclization to 3-arylamino-2,3-dihydrobenzofuran derivatives in the presence of indium under aqueous conditions at ambient temperature in good yields. © 2001 Elsevier Science Ltd.

Metrics

1 Record Views

Details

Title: Indium-mediated tandem dimerization and cyclization of nitrqones and aldimines to 3-arylaminodihydrobenzofurans under aqueous conditions
Creators - without role: Arumugasamy Jeevanandam - National Tsing Hua University
Yong-Chien Ling - Department of Chemistry , National Tsing Hua University
Publication Details: Tetrahedron Letters, Vol.42(26), pp.4361-4362
Identifiers: 9957775063306774
Academic Unit: National Tsing Hua University
Language: English
Resource Type: Journal article

Indium-mediated tandem dimerization and cyclization of nitrqones and aldimines to 3-arylaminodihydrobenzofurans under aqueous conditions

Abstract

Related links

Metrics

Details

National Tsing Hua University Social media