A convenient synthesis of L-ribose from D-fructose

被引：25
|
作者：
Perali, Ramu Sridhar [1 ]
Mandava, Suresh [1 ]
Bandi, Ramakrishna [1 ]
机构：
[1] Univ Hyderabad, Sch Chem, Hyderabad 500046, Andhra Pradesh, India
来源：
TETRAHEDRON | 2011年 / 67卷 / 22期
关键词：
L-Sugars; L-Ribose; D-Fructose; Stereoselective synthesis; HEPATITIS-B-VIRUS; PRACTICAL SYNTHESIS; STEREOSPECIFIC SYNTHESIS; HUMAN-IMMUNODEFICIENCY; EFFICIENT SYNTHESIS; MOLYBDATE IONS; L-NUCLEOSIDES; ANALOG;
D O I：
10.1016/j.tet.2011.04.012
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
An efficient method for the stereoselective synthesis of L-ribose was accomplished starting from commercially inexpensive D-fructose. The intermediates in the process can serve as versatile precursors for the preparation of L-nucleoside analogues. (C) 2011 Elsevier Ltd. All rights reserved.
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页码：4031 / 4035
页数：5
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