Title of article
Convenient ‘one-pot’ synthesis of 3,4-substituted tetrahydrothiophenes through tandem Michael–Henry and Michael–Michael reactions
Author/Authors
Barco، نويسنده , , Achille and Baricordi، نويسنده , , Nikla and Benetti، نويسنده , , Simonetta and De Risi، نويسنده , , Carmela and Pollini، نويسنده , , Gian Piero، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2006
Pages
4
From page
8087
To page
8090
Abstract
In situ generated nitro alkenes underwent tandem Michael–Henry and Michael–Michael sequences leading to the ‘one-pot’ formation of 3,4-substituted tetrahydrothiophenes using the commercially available 1,4-dithiane-2,5-diol (the dimer of mercaptoacetaldehyde) or its 4-mercapto-2-butenoates derivatives as suitable bifunctional partners, respectively.
Keywords
Tandem reactions , Henry reactions , Tetrahydrothiophenes , Michael reactions
Journal title
Tetrahedron Letters
Serial Year
2006
Journal title
Tetrahedron Letters
Record number
1853161
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