Title of article
Aza-Michael reaction promoted by aqueous sodium carbonate solution
Author/Authors
Tang، نويسنده , , Xiao-Ji and Yan، نويسنده , , Zhao-Lei and Chen، نويسنده , , Wen-Liang and Gao، نويسنده , , Ya-Ru and Mao، نويسنده , , Shuai and Zhang، نويسنده , , Yan-Lei and Wang، نويسنده , , Yong-Qiang، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
5
From page
2669
To page
2673
Abstract
A general and efficient aza-Michael reaction promoted by aqueous sodium carbonate solution has been developed. The reaction has complete mono-alkylation selectivity and proceeds with complete chirality retention for chiral amino esters. With a broad substrate scope, a well-common catalyst and simple operation, the catalytic approach provides a facile, practicable, economical, and environmentally benign method for the synthesis of β-amino carbonyl compounds.
Keywords
Aqueous sodium carbonate solution , Aza-Michael reaction , ?-Amino carbonyl compounds , Mono-alkylation
Journal title
Tetrahedron Letters
Serial Year
2013
Journal title
Tetrahedron Letters
Record number
1884478
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