Title of article :
A new approach to 2,2-disubstituted chromenes and tetrahydroquinolines through intramolecular cyclization of chiral 3,4-epoxy alcohols
Author/Authors :
Jean-Yves Goujon، نويسنده , , Françoise Zammattio، نويسنده , , Jean-Mathieu Chrétien، نويسنده , , Isabelle Beaudet، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
13
From page :
4037
To page :
4049
Abstract :
An efficient route to chiral chromene and tetrahydroquinoline ring models and was developed by means of the vanadium epoxidation of chiral homoallylic alcohols and followed by an intramolecular epoxide opening of 3,4-epoxy alcohols and . The configuration of all compounds was confirmed using NMR analysis.
Keywords :
chromene , 2H-1-Benzopyrane , tetrahydroquinoline
Journal title :
Tetrahedron
Serial Year :
2004
Journal title :
Tetrahedron
Record number :
1085429
Link To Document :
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