A convenient method for regioselective C‐5 halogenation of 4(3H)‐oxo‐7H‐pyrrolo[2,3‐d]pyrimidines
- 1 September 1994
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 31 (5), 1181-1183
- https://doi.org/10.1002/jhet.5570310514
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- A dideazatetrahydrofolate analog lacking a chiral center at C-6: N-[4-[2-(2-amino-3,4-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidin-5yl)ethyl[benzoyl]-L-glutamic acid is an inhibitor of thymidylate synthaseJournal of Medicinal Chemistry, 1992
- Total synthesis of 7-iodo-2′,3′-dideoxy-7-deazapurine nucleosides, key intermediates in the preparation of reagents for the automated sequencing of DNATetrahedron Letters, 1988
- 2′‐Desoxytubercidin – Synthese eines 2′‐Desoxyadenosin‐Isosteren durch PhasentrasferglycosylierungEuropean Journal of Organic Chemistry, 1983
- A study of electrophilic substitution in the pyrrolo[2,3‐d]pyrimidine ringJournal of Heterocyclic Chemistry, 1969
- 2-Alkyl(aryl)- and 2,7-Dimethyl-4-substituted Aminopyrrolo [2,3-d] pyrimidinesThe Journal of Organic Chemistry, 1961