Title of article :
Highly diastereoselective allylation of lactols and their ethers using molecular iodine
Author/Authors :
Yadav، نويسنده , , J.S. and Reddy، نويسنده , , B.V. Subba and Reddy، نويسنده , , A. Srinivas and Reddy، نويسنده , , Ch. Suresh and Raju، نويسنده , , S. Satyanarayana، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Pages :
4
From page :
6631
To page :
6634
Abstract :
Lactols and their ethers undergo smooth allylation with allyltrimethylsilane in the presence of 5 mol % iodine in dichloromethane at −78 °C to afford C-allylfuranosides in good yields and with high diastereoselectivity. The use of iodine makes this method simple, convenient and practical. This is the first report on the allylation of lactols with allyltrimethylsilane using molecular iodine as a catalyst. Enhanced diastereoselectivity is the key feature of this protocol.
Keywords :
Lactols , C-Allylfuranosides , allylation , iodine
Journal title :
Tetrahedron Letters
Serial Year :
2009
Journal title :
Tetrahedron Letters
Record number :
1866733
Link To Document :
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