Efficient reduction of azides to amines with tributylstannane. high-yield syntheses of amino and diamino deoxynucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Azides: their preparation and synthetic uses
2. Reaction of benzoyl azide with tributyltin hydride
3. Facile conversion of azides to amines
4. Nucleic acid related compounds. 64. Synthesis of 2',3'-diazido-2',3'-dideoxyadenosine and 2',3'-diamino-2',3'-dideoxyadenosine from 9-(.beta.-D-arabinofuranosyl)adenine
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1. Nitrogen-Centered Radicals Derived from Azidonucleosides;Molecules;2024-05-14
2. Studies on the Regioselective Rearrangement of Azanorbornanic Aminyl Radicals into 2,8-Diazabicyclo[3.2.1]oct-2-ene Systems;The Journal of Organic Chemistry;2022-12-01
3. Formation of Amines from Azides;Comprehensive Organic Transformations;2018-02-28
4. Investigation of reactions postulated to occur during inhibition of ribonucleotide reductases by 2′-azido-2′-deoxynucleotides;Tetrahedron;2012-07
5. ChemInform Abstract: Nucleic Acid Related Compounds. Part 69. Efficient Reduction of Azides to Amines with Tributylstannane. High-Yield Synthesis of Amino and Diamino Deoxynucleosides.;ChemInform;2010-08-21
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