Nucleic acid related compounds. 23. Transformation of ribonucleoside 2',3'-O-ortho esters into unsaturated and deoxy sugar nucleosides via enol ester-substituted iodo intermediates
- 1 December 1976
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 98 (25) , 8213-8217
- https://doi.org/10.1021/ja00441a054
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- 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
- The synthesis of oligoribonucleotides—IIITetrahedron, 1967
- Purine Nucleosides. XII. The Preparation of 2',3'-Dideoxyadenosine, 2',5'-Dideoxyadenosine, and 2',3',5'-Trideoxyadenosine from 2'-Deoxyadenosine*Biochemistry, 1966
- Action of zinc dust and sodium iodide in N,N-dimethylformamide on contiguous, secondary sulfonyloxy groups: a simple method for introducing nonterminal unsaturationCarbohydrate Research, 1965
- ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEOTIDES .1. FORMATION OF DEOXYCYTIDINE DIPHOSPHATE FROM CYTIDINE DIPHOSPHATE WITH ENZYMES FROM ESCHERICHIA COLI1962