Methyl 3,4-di--acetyl-2-deoxy-2(R)-[1h,3h-2,4-dioxo-1-pyrimidinyl]-2-fluoro-β-D-arabinopyranoside: Novel nucleoside analogues via condensation of -2,2-difluoro methyl glycosides with silylated heterocyclic bases.-Reference-Cited by-同舟云学术

Methyl 3,4-di--acetyl-2-deoxy-2(R)-[1h,3h-2,4-dioxo-1-pyrimidinyl]-2-fluoro-β-D-arabinopyranoside: Novel nucleoside analogues via condensation of -2,2-difluoro methyl glycosides with silylated heterocyclic bases.

Published:1986-01 Issue:28 Volume:27 Page:3219-3222
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

An Seung-Ho,Bobek Miroslav

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Synthesis of -difluorosaccharides

2. Isonucleosides. I. Preparation of methyl 2-deoxy-2-(purin-9-yl)arabinofuranosides and methyl 3-deoxy-3-(purin-9-yl)xylofuranosides

3. Isonucleosides. 2. Purine and pyrimidine derivatives of 1,4-anhydro-2-deoxy-D-arabinitol

4. Oxidation of primary and secondary alcohols in partially protected sugars with the chromium trioxide-pyridine complex in the presence of acetic anhydride

5. Proof of the Structure of Sedoheptulosan as 2,7-Anhydro-β-D-altroheptulopyranose1

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