Title of article
Radical cyclisation mediates the synthesis of a new base-ribose carbon bridged adenosine
Author/Authors
Lang، نويسنده , , Pascal and Mayer، نويسنده , , Alain and Jung، نويسنده , , Pierre and Tritsch، نويسنده , , Denis and Biellmann، نويسنده , , Jean-François and Burger، نويسنده , , Alain، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
3
From page
4013
To page
4015
Abstract
Reaction of tributylstannyl, radical generated in situ with AIBN, with (2′,5′-di-O-tert-butyldimethylsilyl-3′-C-ethynyl-β-d-ribo-furanosyl)adenine (5) gave in 69% yield the new conformationally locked nucleosides 6 (E/Z).
Keywords
nucleoside , deaminase , adenosine , Locked , Conformation , radical , tributyltin hydride , AIBN , purinergic receptors
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1841637
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