Title of article
An efficient and extremely mild method for protecting alcohols as 2-tetrahydrofuranyl ethers
Author/Authors
Sean P and Barks، نويسنده , , Jenny M and Gilbert، نويسنده , , Bruce C and Parsons، نويسنده , , Andrew F and Upeandran، نويسنده , , Bala، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
4
From page
6249
To page
6252
Abstract
Reaction of primary or secondary alcohols with BrCCl3 and tetrahydrofuran, usually in the presence of 2,4,6-collidine, leads to the formation of 2-tetrahydrofuranyl ethers in good to excellent yield (56–92%). The reaction mechanism is believed to involve a free-radical chain reaction.
Keywords
acetals , protecting groups , radicals and radical reactions , Oxygen heterocycles
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1638393
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