Selektive 7‐Glykosylierung von 4‐Amino‐7 H‐pyrrolo[2,3‐d]pyrimidin zu Ara‐Tubercidin und dessen α‐Anomer
- 1 January 1981
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 93 (1) , 105-106
- https://doi.org/10.1002/ange.19810930121
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- 4‐Amino‐7‐(β‐D‐arabinofuranosyl)pyrrolo[2,3‐d]pyrimidin — die Synthese von Ara‐Tubercidin durch PhasentransferkatalyseEuropean Journal of Inorganic Chemistry, 1980
- Bevorzugte β-Glycosidbildung durch Phasentransfer-Katalyse bei der Synthese vonD-Arabinofuranosyl-7-desazapurinnucleosidenAngewandte Chemie, 1979
- Fortschritte der Phasentransfer-KatalyseAngewandte Chemie, 1977
- Advances in Phase‐Transfer Catalysis [New synthetic methods (20)]Angewandte Chemie International Edition in English, 1977
- Nucleic acid related compounds. 25. Syntheses of arabino, xylo, and lyxo-anhydro sugar nucleosides from tubercidin ribo-epoxideCanadian Journal of Chemistry, 1977
- STUDIES ON THE BIOCHEMICAL BASIS FOR THE ANTIVIRAL ACTIVITIES OF SOME NUCLEOSIDE ANALOGS*Annals of the New York Academy of Sciences, 1975
- Phase‐Transfer Catalyzed Two‐Phase Reactions in Preparative Organic ChemistryAngewandte Chemie International Edition in English, 1974
- Phasentransfer‐katalysierte Zweiphasenreaktionen in der präparativen organischen ChemieAngewandte Chemie, 1974
- Separation of Nucleoside Mixtures on Dowex-1 (OH-)1Journal of the American Chemical Society, 1965
- 2,3,5-Tri-O-benzyl-D-ribosyl and -L-arabinosyl BromidesThe Journal of Organic Chemistry, 1961