Title of article
Regioselective construction of polysubstituted pyridine ring from Baylis–Hillman adducts via sequential introduction of tosylamide, Michael reaction, aldol condensation, and elimination of TsH
Author/Authors
Park، نويسنده , , Da Yeon and Lee، نويسنده , , Mi Jung and Kim، نويسنده , , Taek Hyeon and Kim، نويسنده , , Jae Nyoung، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
5
From page
8799
To page
8803
Abstract
Facile synthetic method of polysubstituted pyridine derivatives was developed starting from the Baylis–Hillman adducts. The reaction involved sequential introduction of tosylamide, Michael addition, aldol condensation, elimination of p-toluenesulfinic acid, and isomerization process.
Keywords
pyridines , cyclization , Michael reaction , Baylis–Hillman adducts
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1847862
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