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一种合成洛德诺辛(FddA)的工业方法。

An industrial process for synthesizing Lodenosine (FddA).

作者信息

Izawa Kunisuke, Takamatsu Satoshi, Katayama Satoshi, Hirose Naoko, Kozai Shigetaka, Maruyama Tokumi

机构信息

AminoScience Laboratories, Ajinomoto Co., Inc., Kawasaki-ku, Kawasaki, Japan.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):507-17. doi: 10.1081/NCN-120021951.

DOI:10.1081/NCN-120021951
PMID:14565226
Abstract

Two industrial synthetic approaches to Lodenosine (1, FddA, 9-(2,3-dideoxy-2-fluoro-beta-D-threo-pentofuranosyl) adenine) via a purine riboside or a purine 3'-deoxyriboside are described. Several novel applications of deoxygenation and fluorination methods are compared considering reaction yields, economy, safety and environmental concerns.

摘要

描述了两种通过嘌呤核糖苷或嘌呤3'-脱氧核糖苷合成洛德诺辛(1,FddA,9-(2,3-二脱氧-2-氟-β-D-苏式-戊呋喃糖基)腺嘌呤)的工业合成方法。考虑到反应产率、经济性、安全性和环境问题,比较了脱氧和氟化方法的几种新应用。

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