ライフサイエンスコーパス: carbon disulfide

1 iynes with isocyanates, isothiocyanates, and carbon disulfide.

2 n to electrocatalytically reduce protons and carbon disulfide.

3 o catalyze the reaction between epoxides and carbon disulfide.

4 membranes were treated with formaldehyde or carbon disulfide.

5 hase ultraviolet irradiation of a precursor, carbon disulfide.

6 I) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3-methylthiophene,

7 Carbon disulfide, a potentially therapeutic small molecu

8 dendrons were found to be readily soluble in carbon disulfide, a solvent of high polarizability.

9 alkyl-substituted isothiocyanates instead of carbon disulfide afforded the corresponding trifluoromet

10 folds bearing quaternary carbon centers from carbon disulfide and alpha-tertiary propargylamines.

11 by lithium diisopropylamide and reacted with carbon disulfide and methyl iodide to afford a dihydroth

12 ion of xanthate salt through the reaction of carbon disulfide and potassium tert-butoxide is essentia

13 isocyanates, isothiocyanates, carbodiimides, carbon disulfide, and carbon dioxide with carbanions or

14 h neutral reagents including carbon dioxide, carbon disulfide, and nitric oxide.

15 n, the fumigant mixture carbon-tetrachloride/carbon disulfide, and the fungicide chlorothalonil, resp

16 the Stec reaction of phosphorus amides with carbon disulfide; and (2) the one-pot synthesis of thiop

17 ates from para-quinone methides, amines, and carbon disulfide are described under catalyst and additi

18 In contrast, phenylnitrene anion reacts with carbon disulfide by C+ or CS+ abstraction, forming S- or

19 , and related thiocarbonyl compounds such as carbon disulfide, certain substituted thiourea derivativ

20 e (H2S), methanethiol, dimethyl sulfide, and carbon disulfide concentrations.

21 V)O vibrates at a frequency of 986 cm(-1) in carbon disulfide, consistent with a triply bonded Cr(V)[

22 molecules with narrow Doppler lines, such as carbon disulfide (CS(2)) and its three isotopologues.

23 persulfides, both carbonyl sulfide (COS) and carbon disulfide (CS(2)) have been postulated to be pote

24 carbonyl sulfide (OCS), dimethylsulfide, and carbon disulfide (CS(2)) in the breath of a group of cys

25 of aziridines with carbon dioxide (CO(2)) or carbon disulfide (CS(2)) under mild conditions.

26 quenching of nitrogenase during reduction of carbon disulfide (CS(2)) was previously shown to result

27 ghly sensitive to the volatile semiochemical carbon disulfide (CS(2)), a component of rodent breath a

28 sulfide (DMS) and less clearly iodomethanes, carbon disulfide (CS(2)), and isoprene, while the LMA sp

29 ented here has the goal of examining whether carbon disulfide (CS2) may play a role as an endogenousl

30 ) coating was used for trimethylamine (TMA), carbon disulfide (CS2), dimethylsulfide (DMS), and dimet

31 mental and theoretical study of core-ionized carbon disulfide (CS2), we demonstrate that it is possib

32 Irradiation of gaseous carbon disulfide [CS2(g)] at 313 nanometers produces a d

33 We identified carbon disulfide, dimethyl sulfide, methionol and benzot

34 In this study, the release of acetone, carbon disulfide, dimethyl sulfide, nitromethane, pentan

35 oic, pentanoic acids, benzaldehyde, ethanal, carbon disulfide, dimethyldisulfide, acetone, 2-butanone

36 Carbon disulfide exposure leads to an identical axonopat

37 spectrometry to investigate the dynamics in carbon disulfide following the interaction with an inten

38 transformations of organic compounds (e.g., carbon disulfide, halogenated organic compounds).

39 ion of an unprecedented decameric capsule in carbon disulfide, held together by the combination of do

40 nsation of dioctylamine or didecylamine with carbon disulfide in anhydrous ethanol and compared to al

41 prepared by reaction of alcohols/thiols with carbon disulfide in the presence of bases.

42 by reaction of primary/secondary amines with carbon disulfide in the presence of bases.

43 precursor inks were synthesized using known carbon disulfide insertion chemistry to create Group 4 m

44 Carbon disulfide is a suitable solvent for these reactio

45 Typical examples of substrates include carbon disulfide, methyl dithioacetate, methyl dithioben

46 cycloaddition of 2-acylethynylpyrroles with carbon disulfide (NaOH, DMSO, room temperature) proceeds

47 adiation (Hg--Xe arc source) of liquid-phase carbon disulfide produces a new carbon--sulfur polymer w

48 this compound with either carbon dioxide or carbon disulfide results in insertion into the uranium-c

49 In this study we demonstrate that in carbon disulfide the chiral decameric cavity aggregate c

50 steps from chalcones and then condense with carbon disulfide to afford 8-azachromones containing a m

51 uperconducting phase observed in diamagnetic carbon disulfide under high pressure.

52 rapid synthesis of isothiouronium salts from carbon disulfide under microwave irradiation, allowing t

53 nced four-wave mixing in dilute solutions of carbon disulfide using an ultrafast (< or = 1 ps) laser

54 The vinylidene ketenes react with carbon disulfide via a four-membered thiete intermediate