Efficient Synthesis of Methylenebis(phosphonate) Analogues of P1,P2-Disubstituted Pyrophosphates of Biological Interest. A Novel Plausible Mechanism
- 1 April 1997
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (16) , 3691-3695
- https://doi.org/10.1021/ja964058i
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Synthesis of thiazole-4-carboxamide-adenine difluoromethylenediphosphonates substituted with fluorine at C-2′ of the adenosineCarbohydrate Research, 1993
- Synthesis of thiazole-4-carboxamide adenine dinucleotide (TAD) analogues with an altered anhydride bridgeCollection of Czechoslovak Chemical Communications, 1993
- Thiazole-4-carboxamide adenine dinucleotide (TAD). Analogs stable to phosphodiesterase hydrolysisJournal of Medicinal Chemistry, 1986
- Synthesis of thiazole-4-carboxamide adenine dinucleotide. A powerful inhibitor of IMP dehydrogenaseJournal of Medicinal Chemistry, 1983
- Phosphonates as analogues of natural phosphatesChemical Reviews, 1977
- IMP dehydrogenase, an enzyme linked with proliferation and malignancyNature, 1975
- Cyclization of the Phosphate Side Chain of Adenosine Triphosphate: Formation of Monoadenosine 5′-TrimetaphosphateScience, 1974
- Reactions of hexaborane(10) with molecular Lewis bases. Proton abstraction and molecular additionJournal of the American Chemical Society, 1970
- The Molecular Constitution of Methyl and Ethyl Polyphosphate and the Langheld Esters1Journal of the American Chemical Society, 1966