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1 otocols could be enhanced by the presence of cyclohexylamine.
2 n of 1 with 254 nm light in cyclohexane gave cyclohexylamine 11, diamine 3c, and azobenzene 12 as the
3 ture of the major adduct between [Pt(ammine)(cyclohexylamine)]2+ and a DNA dodecamer, using the same
6 ,2R-diaminocyclohexane)](2+), cis-[Pt(NH(3))(cyclohexylamine)](2+), [Pt(ethylenediamine)](2+), cis-[P
7 the cellular processing of cis-[Pt(NH(3))- (cyclohexylamine)](2+), but not [Pt((1R,2R)-diaminocycloh
10 Protected alpha-guanidino acids coupled to cyclohexylamine and trans-1,4-diaminocyclohexane in good
12 piperidine 4, we developed a novel series of cyclohexylamine- and piperidine-based benzenesulfonamide
13 Co(2)(CO)(8), in DME and in the presence of cyclohexylamine, are sufficient for the cyclocarbonylati
14 synthesized with 75 % conversion from 10 mM cyclohexylamine by employing whole-cell biocatalysts.
15 tiodeprotonation or deuteriodeprotonation in cyclohexylamine catalyzed by cesium cyclohexylamide.
17 e sequential hydrogenation of nitroarenes to cyclohexylamines compared with its mono/bi-metallic coun
20 re improved resolution was the separation of cyclohexylamine (K(0) = 1.83) and 2-hexanone (K(0) = 1.8
21 ain 1,2-intrastrand cross-links in which the cyclohexylamine ligand is directed toward the 3'-end of
22 oxaliplatin, and (Bis-aceto-ammine-dichloro-cyclohexylamine-platinum(IV) (JM216), are repaired in vi