The role of N-acetylcycloserine in the acyl transfer reactions
The ability of α-N-acetylcycloserine to participate in acyl transfer reactions has been investigated. The reaction with cinnamoylimidazole yields a stable monocinnamoyl intermediate, while that with p-nitrophenyl acetate yields a derivative which undergoes facile deacylation. The kinetics of acylation of α-N-acetylcycloserine and of the deacylation of its acetyl intermediate are reported.
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Strain effects in acyl transfer reactions. Part I. The kinetics of hydrolysis of some N-aryl-lactams
1972 ◽
pp. 1366
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1973 ◽
pp. 981
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1995 ◽
Vol 1251
(2)
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pp. 191-197
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1968 ◽
Vol 90
(13)
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pp. 3478-3486
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1970 ◽
Vol 92
(22)
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pp. 6575-6588
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