Title of article :
Regio- and stereoselective ring-opening of epoxides using organic dithiophosphorus acids as nucleophiles
Author/Authors :
Li، نويسنده , , Zhaoming and Zhou، نويسنده , , Zhenghong and Li، نويسنده , , Kangying and Wang، نويسنده , , Lixin and Zhou، نويسنده , , Qilin and Tang، نويسنده , , Chuchi Tang، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
3
From page :
7609
To page :
7611
Abstract :
A practical method for the synthesis of β-hydroxymercaptans has been successfully developed through the ring-opening of epoxides with organic dithiophosphorus acids 1. Highly regio- and stereoselective products, β-hydroxyalkyl dithiophosphates, which were transformed to the corresponding synthetically valuable β-hydroxymercaptans by further reduction, were obtained under mild reaction conditions without any catalyst or promoter. Highly enantioselective ring-opening reaction of cyclohexene epoxide with 1 was realized in the presence of a chiral (salen)Ti(IV) complex.
Journal title :
Tetrahedron Letters
Serial Year :
2002
Journal title :
Tetrahedron Letters
Record number :
1658577
Link To Document :
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