ライフサイエンスコーパス: nitro compound

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1 y facile dealkylation to release the primary nitro compound.

2 n the formal cyclopropanation of an aromatic nitro compound.

3 te O2 for oxidation of the aryl amine to the nitro compound.

4 number of other aromatic and heteroaromatic nitro compounds.

5 s, alpha-cyano esters, beta-keto esters, and nitro compounds.

6 of chiral alkoxy aldehydes with a series of nitro compounds.

7 r 20-microL injections of nonpreconcentrated nitro compounds.

8 sted acid and second order dependence in the nitro compounds.

9 dole-3-acetaldoxime to the corresponding aci-nitro compound, 1-aci-nitro-2-indolyl-ethane, with a K(m

10 The nitro compound 12 was found to have even higher H(3) rec

11 The nitro compound 3l is prepared in 91% yield by nitration

12 , which were obtained from the corresponding nitro compounds 6 and 7 respectively, by reduction of th

13 he sigma-1 site, whereas the corresponding o-nitro compound 9 shows the highest affinity for the sigm

14 ighting the differences in the metabolism of nitro compounds among mycobacterial species and emphasiz

15 t higher order hydrogen-bonded aggregates of nitro compounds and acids are the kinetically competent

16 sfully applied to the reduction of aliphatic nitro compounds and azides.

17 with excellent discrimination against other nitro compounds and heavy metals.

18 hiles to give the corresponding butenolides, nitro compounds, and alpha-substituted tetrahydroisoquin

19 Despite the fact that azides, nitro compounds, and amines do lead to the formation of

20 Unactivated allylic nitro compounds do not spontaneously release nitrite and

21 The aci-nitro compound formed reacts non-enzymatically with thio

22 nzymatic route for the synthesis of aromatic nitro compounds from their corresponding aromatic amines

23 red QSAR of bacterial reduction of different nitro compounds giving a Hammett correlation with rho=0.

24 We conclude that disulfide and nitro compounds have an unexploited potential for use in

25 Nitro compounds have long been known to dissociate to gi

26 man feces, whereas tocopherol only decreased nitro compounds in rats and lipoperoxidation in feces of

27 ions into this surprising effect reveal that nitro compounds induce a switch from first order concent

28 -NH2, -NHCH3, and -OH) to the corresponding nitro compounds is described by use of nonanebis(peroxoi

29 A cocatalytic effect of nitro compounds is described for the B(C6F5)3.H2O cataly

30 lyzing the transfer hydrogenation from AB to nitro compounds, leading to the green synthesis of quina

31 functionalized boron compounds (boron azide, nitro compound, nitrous ester, etc.).

32 applicable, as it is capable of determining nitro compounds of interest (e.g., nitroglycerin) that h

33 uctase A catalyzes the divalent reduction of nitro compounds, quinones, and dyes by NADPH.

34 ng attendant upon the univalent reduction of nitro compounds, quinones, and dyes.

35 Condensation of aldehyde (S)-(-)-17 with nitro compound (S)-(-)-27, both of which were prepared f

36 method allows for the synthesis of aromatic nitro compounds that cannot be accessed efficiently via

37 tion (330 < lambda < 500 nm) of the nitrosyl-nitro compound (TPP)Fe(NO)(NO(2)) (TPP = tetraphenylporp

38 atic carboxylic acids to their corresponding nitro compounds using nitronium tetrafluoroborate and si

39 Allylic nitro compounds were synthesized and evaluated as organi

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