Facile conversion of adenosine into new 2′-substituted-2′-deoxy-arabinofuranosyladenine derivatives: Stereospecific syntheses of 2′-azido-2′-deoxy-,2′-amino-2′- deoxy-, and 2′-mercapto-2′-deoxy-β-d-arabinofuranosyladenines-Reference-Cited by-同舟云学术

Facile conversion of adenosine into new 2′-substituted-2′-deoxy-arabinofuranosyladenine derivatives: Stereospecific syntheses of 2′-azido-2′-deoxy-,2′-amino-2′- deoxy-, and 2′-mercapto-2′-deoxy-β-d-arabinofuranosyladenines

Published:1978-01 Issue:45 Volume:19 Page:4341-4344
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ranganathan R.,Larwood D.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Modification of the 2′-position of purine nucleosides: syntheses of 2′-α-substituted-2′-deoxyadenosine analogs

2. A general method for the synthesis of 2'-azido-2'-deoxy- and 2'-amino-2'-deoxyribofuranosyl purines

3. Studies of nucleosides and nucleotides—LXXIV

4. Nucleosidtransformationen, 2: Selektive Oxiranringöffnung von 9‐(2,3‐Anhydro‐β‐ D ‐ribofuranosyl)‐ und 9‐(2,3‐Anhydro‐β‐ D ‐lyxofuranosyl)adenin

5. Synthesis of some pyrimidine 2'-amino-2'-deoxynucleosides

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