A facile synthesis of 2-deoxy-2-hydroxymethyl-β-D-erythrofuranosyl nucleosides from 9-(2-deoxy-2-hydroxymethyl-β-D-erythrooxetanosyl)adenine by a novel ring expansion accompanying transglycosidation-Reference-Cited by-同舟云学术

A facile synthesis of 2-deoxy-2-hydroxymethyl-β-D-erythrofuranosyl nucleosides from 9-(2-deoxy-2-hydroxymethyl-β-D-erythrooxetanosyl)adenine by a novel ring expansion accompanying transglycosidation

Published:1989-01 Issue:17 Volume:30 Page:2269-2270
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kato Kuniki,Minami Takae,Takita Tomohisa,Nishiyama Shigeru,Yamamura Shosuke,Naganawa Hiroshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference9 articles.

1. The Role of the 5′-Hydroxyl Group of Adenosine in Determining Substrate Specificity for Adenosine Deaminase

2. Branched-Chain Sugar Nucleosides. A New Type of Biologically Active Nucleoside

3. Branched chain sugars. The synthesis of adenine nucleosides of 3- deoxy-3-C-hydroxymethyl-D-erythrofuranose and 2-deoxy-2-C- hydroxymethyl-D-erythrofuranose

4. Oxetanocin, a novel nucleoside from bacteria.

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