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1 prolactone, a cyclic carbonate, and a cyclic phosphoester.
2 mediated nucleophilic attack by water on the phosphoester.
3 d is not inhibited by Etn, choline, or their phosphoesters.
4 er than those of the six-membered monocyclic phosphoester, 2-ethoxy-1,3,2-dioxaphosphinane 2-oxide.
5 d subsequent deprotection of the cyano ethyl phosphoester afforded the target compounds in 16-21 % ov
6 uctures and mechanistic requirements between phosphoesters and peptides during hydrolysis, the study
8 ter oxygen, such that diverse aryl and alkyl phosphoesters are turned over with similar catalytic eff
10 sphopantetheine swinging arm bound through a phosphoester bond to Ser(354) of the intermediate domain
11 redox-active prosthetic groups attached by a phosphoester bond to threonine residues in subunits NqrB
12 it cleaves a pyrophosphate bond instead of a phosphoester bond, and its substrate contains nucleoside
13 ecule to the phosphorus atom of the scissile phosphoester bond, with the attacking water being simult
18 or a closely related analog to catalyze RNA phosphoester cleavage, producing a rate enhancement of a
20 Qualitatively, the outcome is determined by phosphoester elongation and siloxane contraction along t
23 ructures provide models for intermediates in phosphoester hydrolysis and suggest specific mechanistic
24 bitors toward the hydrolysis of the peptide, phosphoester hydrolysis by peptidases is thus not expect
26 er of a large class of enzymes that catalyze phosphoester hydrolysis using a phosphoaspartate-enzyme
29 edominantly C2'-endo to C3'-endo when the 3'-phosphoester is replaced by a phosphoramidate group.
33 ecules in solution populate a wider range of phosphoester ring conformations than in R32 and P3 cryst
34 al modeling of the six-membered 3',5'-cyclic phosphoester ring derived from deoxyribose indicated str
37 se library of hyperbranched unsaturated poly(phosphoester)s that allow efficient scavenging of single
39 ns involving inorganic phosphate and organic phosphoesters such as phospholipids, phosphorylated prot
40 at 821 cm-1is demonstrated as diagnostic of phosphoester torsions alpha and zeta in the gauche+ rang
41 ozyme promotes self-cleavage via an internal phosphoester transfer reaction involving the adjacent 2'
46 w DSPs accomplish similar reaction rates for phosphoesters, whose reactivity (i.e., pK(a) of the leav
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