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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
8 alytic reactions, such as hydrogen exchange, alcoholysis and aminolysis, hydrogen evolution, hydrogen
9 ether integrase was catalyzing hydrolysis or alcoholysis and were not influenced by the particular ex
11 se of asymmetric induction of the asymmetric alcoholysis but also provides a rationale on how the cat
12 der anhydrous conditions, MsAcT demonstrates alcoholysis in substantially aqueous media and, in the p
15 ental results revealed that enantioselective alcoholysis of 3-substituted glutaric anhydrides afforde
17 yromellitate (31b), itself prepared from the alcoholysis of benzyl pyromellitate triacid chloride (30
24 uoride-promoted heterogeneous hydrolysis and alcoholysis of various organo-phosphorus (OP) compounds
27 ndicate that the cinchona alkaloid-catalyzed alcoholysis proceeds by a general base catalysis mechani
28 A-EE) and vanillyl alcohol by a solvent-free alcoholysis process catalysed by Candida antarctica lipa
31 minimize their breaking up via hydrolysis or alcoholysis reactions, and the linking at defined positi
32 sis features a base-catalyzed alkynyl silane alcoholysis/ring-closing enyne metathesis sequence for f
33 ng, joining, disintegration, and nonspecific alcoholysis) that differ in specificity for the attackin
36 were readily prepared from [(PNP)M(CH3)3] by alcoholysis with HOAr, undergo photolytically induced al
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