Title of article
Enantioselective straightforward access to benzo[b]thiophene analogs of Azatoxin
Author/Authors
Gracia، نويسنده , , Stéphanie and Marion، نويسنده , , Cédric and Rey، نويسنده , , Jullien and Popowycz، نويسنده , , Florence and Pellet-Rostaing، نويسنده , , Stéphane and Lemaire، نويسنده , , Marc، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
4
From page
3165
To page
3168
Abstract
Horner-Wadsworth Emmons olefination followed by asymmetric hydrogenation allowed the first synthetic access to the chiral thiotryptophan with good enantiomeric excess. Oxazolidinone formation followed by a Pictet–Spengler condensation provided the benzothiophenic analog of Azatoxin.
Keywords
Azatoxin , Oxazolidininone , Benzothiophene , Pictet–Spengler Cylization , Chiral thiotryptophan
Journal title
Tetrahedron Letters
Serial Year
2012
Journal title
Tetrahedron Letters
Record number
1880994
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