NMR chemical shifts and one-bond ' 3C-1 H couplings are reported for B'azido-3'-deoxythymidine, 2',3'-dideoxyadenosine, 2',3'-dideoxycytidine and 2 ' 3dideoxyinosine. Unambiguous assignments were made on the basis of results from 2D INADEQUATE experiments to establish the carbon-carbon connectivitie
Synthesis and biological evaluation of dinucleoside methylphosphonates of 3′-azido-3′-deoxythymidine and 2′, 3′-dideoxycytidine
✍ Scribed by Frédéric Puech; Gilles Gosselin; Jan Balzarini; Steven S. Good; Janet L. Rideout; Erik De Clercq; Jean-Louis Imbach
- Book ID
- 118001256
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 679 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0166-3542
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## Abstract New approaches to the synthesis of 3′‐azido‐3′‐deoxythymidine labelled with tritium in the heterocyclic base have been developed. With this aim, enzymatic transribosylation with [^3^H]thymine using the enzyme preparation from rat liver and a three‐step chemical synthesis with use of the
The new monomer, 5@-O-methacryloyl-3@-azido-3@-deoxythymidine (MAZT), was synthesized by the reaction of methacryloyl chloride and 3@-azido-3@-deoxythymidine (AZT). Poly(MAZT) and copolymers of MAZT with vinyl acetate (VAc) and maleic anhydride (MAH) were synthesized by radical polymerizations. The