Title of article
Efficient synthesis of β-enaminoesters via highly stereoselective Reformatsky reaction with disubstituted formamides as novel electrophiles
Author/Authors
Ke، نويسنده , , Yi-Yin and Li، نويسنده , , Yu-Jin and Jia، نويسنده , , Jian-Hong and Sheng، نويسنده , , Wei-Jian and Han، نويسنده , , Liang and Gao، نويسنده , , Jian-Rong، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2009
Pages
3
From page
1389
To page
1391
Abstract
An efficient synthesis of various β-enaminoesters has been achieved via Reformatsky reaction with disubstituted formamides as novel electrophiles. The exclusive β-enaminoester E-isomers were obtained in 60–72% yield.
Keywords
?-enaminoesters , Reformatsky reaction , stereoselective , Disubstituted formamides
Journal title
Tetrahedron Letters
Serial Year
2009
Journal title
Tetrahedron Letters
Record number
1862951
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