Synthesis, activation, and cytotoxicity of aldophosphamide analogs
RF Borch, RR Valente
Index: Borch, Richard F.; Valente, Ronald R. Journal of Medicinal Chemistry, 1991 , vol. 34, # 10 p. 3052 - 3058
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Citation Number: 25
Abstract
A series of perhydrooxazine analogues of aldophosphamide has been prepared, and their slP NMR kinetics and in vitro cytotoxicity have been evaluated. These compounds were developed on the basis of the idea that ring opening and tautomerization to an enamine intermediate might provide a mechanistic alternative to the &elimination reaction for release of phosphoramide mustard. The 4, 4, 6-trimethyltetrahydro-l, 3-oxazine moiety was ...
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