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1 lding chiral cyclohexadienes, which are then aromatized.
3 steroid 19-nortestosterone, are individually aromatized and reduced to the corresponding saturated ke
4 ng of the ring H abstraction pathway between aromatized and ring hydroxylated products is due to the
5 ng five-, six-, and seven-membered rings are aromatized benzothiophene products, whereas eight- and t
8 inding mode of its substrate, namely the non-aromatized coumaryl-trione intermediate of the chalcone
10 se compounds represent the first examples of aromatized diboraacenes where the boron atoms are spatia
14 dibromopentacene precursor that can be fully aromatized in a final step through a DDQ-mediated dehydr
16 her, 13,14-dehydro benzophenanthridines were aromatized into biologically important benzophenanthridi
18 ment of adult ovariectomized females with an aromatized metabolite of testosterone, estradiol, for 8
19 ressant-like effects of testosterone and its aromatized metabolite, estradiol, were then investigated
20 e bonds, NSen(2)B; and the b-ring completely aromatized, NSarB) were incorporated into the steroid sp
22 ing hydroxylated product, CHDEA-6OH, and the aromatized product, PEA, at the carbon-oxygen bond forma
23 ino-1-(1, 4-cyclohexadienyl)ethanol, and the aromatized product, phenylethylamine, and that the two p
29 aromatic, anthracene core products or fully aromatized to 3,9-dialkyloxyperylenes in good yields.
33 to androgen receptors (AR), they may also be aromatized to estrogens and thus potentially impart effe
34 to the conclusion that testicular androgens aromatized to estrogens are neuroprotective in males and
42 nd aroma compound concentration in emulsions aromatized with (-)-alpha-pinene than with diacetyl.