ライフサイエンスコーパス: nitro compound

1 n the formal cyclopropanation of an aromatic nitro compound.

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

3 y facile dealkylation to release the primary nitro compound.

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

5 number of other aromatic and heteroaromatic nitro compounds.

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

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

8 r 20-microL injections of nonpreconcentrated nitro compounds.

9 xy- and azo-aromatics from the corresponding nitro compounds.

10 These amines are often sourced from nitro compounds.

11 emoselective access to a variety of aromatic nitro compounds.

12 egacy and emerging MCs and potentially other nitro compounds.

13 )(2)]-mu-oxo precatalyst in the reduction of nitro compounds.

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

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

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

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

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

19 found that it is efficient in reducing other nitro compounds also such as Picric acid and Nitrobenzen

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

21 ed SBA sample is mixed with NaOH to obtain a nitro compound and the compound is then dripped onto the

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

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

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

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

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

27 uding unsaturated ketones, esters, sulfones, nitro compounds, and thiolating reagents, as an entry to

28 Nitro compounds are important precursors and intermediat

29 FER suggests that these structurally diverse nitro compounds are reduced by iron oxide-Fe(aq)(2+) cou

30 cascade reduction process in which CO(2) and nitro-compounds are reduced concurrently to yield N-meth

31 ion to be compatible with cheap and abundant nitro-compounds by developing a cascade reduction proces

32 Unactivated allylic nitro compounds do not spontaneously release nitrite and

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

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

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

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

37 Nitro compounds have long been known to dissociate to gi

38 e reduction kinetics of structurally diverse nitro compounds in compositionally complex soils based o

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

40 g the fate and half-lives of MCs and related nitro compounds in reducing environments.

41 cyclics, halogenated compounds, dioxins, and nitro compounds in the molecular mass range of 46-244 Da

42 ldehydes or ketones) with ammonia, amines or nitro compounds in the presence of suitable catalysts an

43 nitriles) or into an amine (for instance, a nitro compound) in the presence of the same reducing age

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

45 he electrochemically-driven hydrogenation of nitro compounds into amines in the hydrogenation compart

46 The hydrogenation of nitro compounds into amines requires harsh reaction cond

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

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

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

50 e, lepidocrocite, and ferrihydrite) and four nitro compounds (NB, CN-NB, Cl-NB, and NTO) from six sep

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

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

53 onyl and carboxylic derivatives, imines, and nitro compounds promoted by iron catalysts.

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

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

56 (2) can be readily transformed into valuable nitro compounds relevant to construction, agrochemical,

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

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

59 paradigm for chemoselective hydrogenation of nitro compounds to amines, under mild, aqueous condition

60 nabled a wide range of commercially relevant nitro compounds to be hydrogenated into amines, without

61 The reduction of nitro compounds to the corresponding amines is one of th

62 The hydrogenation of nitro compounds to their corresponding amines is develop

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

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

65 on non-noble 3d-metals for the reduction of nitro compounds using various reductants.

66 protocol for reductive alkylation of azides/nitro compounds via a borrowing hydrogen (BH) method.

67 Allylic nitro compounds were synthesized and evaluated as organi

68 e (H(3)SiPh), we can chemoselectively reduce nitro compounds while retaining carbonyl functionality.

69 ectrochemical coupling of readily accessible nitro-compounds with benzyl alcohols to yield nitrone de