Efficient reduction of azides to amines with tributylstannane. high-yield syntheses of amino and diamino deoxynucleosides
- 1 October 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (44) , 6293-6296
- https://doi.org/10.1016/0040-4039(91)80150-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- 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)adenineThe Journal of Organic Chemistry, 1991
- Azides: their preparation and synthetic usesChemical Reviews, 1988
- Facile conversion of azides to aminesTetrahedron Letters, 1986
- Transient protection: efficient one-flask syntheses of protected deoxynucleosidesJournal of the American Chemical Society, 1982
- Nucleic acid related compounds. 22. Transformation of ribonucleoside 2',3'-O-ortho esters into halo, deoxy, and epoxy sugar nucleosides using acyl halides. Mechanism and structure of productsJournal of the American Chemical Society, 1976
- Synthesis of some pyrimidine 2'-amino-2'-deoxynucleosidesThe Journal of Organic Chemistry, 1971
- Reaction of benzoyl azide with tributyltin hydrideJournal of Organometallic Chemistry, 1967
- Synthese 5′‐substituierter AdenosinderivateEuropean Journal of Inorganic Chemistry, 1965