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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
7        Target site selection for nonspecific alcoholysis again mapped to the central domain of IN, co
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
10 Mg(2+) and were confirmed with a nonspecific alcoholysis assay.
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
13                                  Nonspecific alcoholysis may provide insights into the structure and
14                                              Alcoholysis of (+/-)-2-phenyl-4-benzyloxazol-5(4H)-one (
15 ental results revealed that enantioselective alcoholysis of 3-substituted glutaric anhydrides afforde
16                                              Alcoholysis of 5 with various phenols/alcohols provides
17 yromellitate (31b), itself prepared from the alcoholysis of benzyl pyromellitate triacid chloride (30
18                                  A selective alcoholysis of dialkynyl silyl ethers to mixed silaketal
19  practical catalyst for the enantioselective alcoholysis of meso cyclic anhydrides.
20 ps in the transition state of the asymmetric alcoholysis of meso cyclic anhydrides.
21 ocessing of viral DNA and during nonspecific alcoholysis of nonviral DNA.
22                                              Alcoholysis of PMDA in CH2Cl2/Et3N led to the formation
23                                              Alcoholysis of the oligomer yields the parent 4,5,6,7,8,
24 uoride-promoted heterogeneous hydrolysis and alcoholysis of various organo-phosphorus (OP) compounds
25               Unlike hydrolases that perform alcoholysis only under anhydrous conditions, MsAcT demon
26 tis forms the mechanistic basis for favoring alcoholysis over hydrolysis in water.
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
29                                              Alcoholysis provided the precursor for 5, ammonolysis at
30                                          The alcoholysis reaction is slowed down for higher alcohols,
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
34 lysis was found as a reversible pathway, and alcoholysis was confirmed to be irreversible.
35                               Hydrolysis and alcoholysis were identified as the major paths for this
36 were readily prepared from [(PNP)M(CH3)3] by alcoholysis with HOAr, undergo photolytically induced al

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