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1 ion of meso cyclic anhydrides via asymmetric alcoholysis.
2 in that these reactions can proceed through alcoholysis.
3 reaction, and 11 are active for nonspecific alcoholysis.
4 se activity which we have termed nonspecific alcoholysis.
5 f hydrolysis and esterification, rather than alcoholysis.
6 and was not predicted by, the site-specific alcoholysis activity previously described for IN at the
9 alytic reactions, such as hydrogen exchange, alcoholysis and aminolysis, hydrogen evolution, hydrogen
10 ether integrase was catalyzing hydrolysis or alcoholysis and were not influenced by the particular ex
13 se of asymmetric induction of the asymmetric alcoholysis but also provides a rationale on how the cat
14 der anhydrous conditions, MsAcT demonstrates alcoholysis in substantially aqueous media and, in the p
17 ental results revealed that enantioselective alcoholysis of 3-substituted glutaric anhydrides afforde
19 e first examples for the study of asymmetric alcoholysis of anhydrides in ionic liquid solution and g
20 yromellitate (31b), itself prepared from the alcoholysis of benzyl pyromellitate triacid chloride (30
22 ings suggest that the phenolic alcohol-based alcoholysis of fish oil offers a promising approach to g
26 his study hypothesizes that the solvent-free alcoholysis of oil recovered from salmon heads using van
31 uoride-promoted heterogeneous hydrolysis and alcoholysis of various organo-phosphorus (OP) compounds
35 ndicate that the cinchona alkaloid-catalyzed alcoholysis proceeds by a general base catalysis mechani
36 A-EE) and vanillyl alcohol by a solvent-free alcoholysis process catalysed by Candida antarctica lipa
38 e describe the acceleration of a bimolecular alcoholysis reaction as a paradigm for IR light-driven g
40 minimize their breaking up via hydrolysis or alcoholysis reactions, and the linking at defined positi
41 sis features a base-catalyzed alkynyl silane alcoholysis/ring-closing enyne metathesis sequence for f
42 ng, joining, disintegration, and nonspecific alcoholysis) that differ in specificity for the attackin
43 of a C5 methyl, which completely blocks C15 alcoholysis via destabilization of an intermediate twist
46 were readily prepared from [(PNP)M(CH3)3] by alcoholysis with HOAr, undergo photolytically induced al