High-yield synthesis of 3′-amino-3′-deoxynucleosides. Conversion of adenosine to 3′-amino-3′-deoxyadenosine-Reference-Cited by-同舟云学术

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High-yield synthesis of 3′-amino-3′-deoxynucleosides. Conversion of adenosine to 3′-amino-3′-deoxyadenosine

Published:1989 Issue:18 Volume:30 Page:2329-2332
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Samano Mirna C.,Robins Morris J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. This communication is “Nucleic Acid Related Compounds. 56.” The previous paper is: M.J. Robins, R. Zou, F. Hansske, D. Madej, and D.L.J. Tyrrell, Nucleos. Nucleot. (in press)

2. 508. Cordycepin, a metabolic product from cultures of Cordyceps militaris(Linn.) link. Part I. Isolation and characterisation

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2. Total Syntheses of a Conformationally LockedNorth-Type Methanocarba Puromycin Analogue and a Dinucleotide Derivative;Chemistry - A European Journal;2009-06-15

3. Synthesis of a xylo-Puromycin Analogue;Synlett;2008-09-10

4. A simple and efficient synthesis of puromycin, 2,2′-anhydro-pyrimidine nucleosides, cytidines and 2′,3′-anhydroadenosine from 3′,5′-O-sulfinylXylo-nucleosides;Nucleosides, Nucleotides and Nucleic Acids;2006-08

5. Synthesis of 1′-Homo-N-nucleosides from Hexitols;European Journal of Organic Chemistry;2003-11

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