Synthetic Study of 1, 2, 3-Tri-O-Acetyl-5-Deoxy-D-Ribofuranose-Reference-Cited by-同舟云学术

Synthetic Study of 1, 2, 3-Tri-O-Acetyl-5-Deoxy-D-Ribofuranose

Published:2013-09 Issue: Volume:781-784 Page:1184-1186
ISSN:1662-8985
Container-title:Advanced Materials Research
language:
Short-container-title:AMR

Author:

Zhang Jian Ting¹,Chen Shi Peng¹,Feng Jun Min¹,Liu Dong Wang¹,Tang Lin Jun¹,Wang Xiao Ji¹,Huang Shuang Ping¹

Affiliation:

1. Jiangxi Science and Technology Normal University

Abstract

A practical synthetic route towards 1,2,3-tri-O-acetyl-5-deoxy-D-ribofuranose from D-ribose is described, which started from D-ribose and proceeded through ketalization,esterification,reduction,hydrolysis and acetylation in more than 30% overall yield.

Publisher

Trans Tech Publications, Ltd.

Subject

General Engineering

Link

https://www.scientific.net/AMR.781-784.1184.pdf

Reference4 articles.

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2. Kissman HM, Baker BR. The synthesis of certain 5-deoxy-D-ribofuranosylpurines [J]. J. Am. Chem. Soc., 1957, 79(20): 5534-5540.

3. Lerner L M. An improved preparation of 5-deoxyadenosine by coupling methods. Carbohydr. Res., 1988, 184: 250-253.

4. Pothukuchi Sairam, Ramachandra Puranik, Bhatraju Sreenivasa Rao et al. Synthesis of 1, 2, 3-tri-O-acetyl-5-deoxy-D-ribofuranose from D-ribose. Carbohydrate Research., 2003, 338, 303-306.

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