ライフサイエンスコーパス: dimethyl sulfide

1 te with levels of isoprene, monoterpenes, or dimethyl sulfide.

2 erexpressing methionine-gamma-lyase produced dimethyl sulfide.

3 on of organosulfur compounds (OSCs), such as dimethyl sulfide.

4 g isoprene, monoterpenes, and very recently, dimethyl sulfide.

5 nisole < ether-sulfides < dialkyl sulfides < dimethyl sulfide.

6 of the ionic liquid on the nucleofugality of dimethyl sulfide.

7 avage pathway to the climatically active gas dimethyl sulfide(3,4).

8 es of domoic acid, a marine algal toxin, and dimethyl sulfide, a volatile precursor to cloud condensa

9 ne adducts were similar to that observed for dimethyl sulfide adducts.

10 Dimethyl sulfide, an alternate substrate for thioether S

11 le volatile organic sulfur compounds such as dimethyl sulfide and (2-methylthio)ethanol.

12 amined as borane carriers in comparison with dimethyl sulfide and 1,4-oxathiane: tert-butyl methyl su

13 of tissue disintegration, and the release of dimethyl sulfide and dimethyl disulfide was related to t

14 The oxidation of dimethyl sulfide and dimethyl selenide, two-electron oxi

15 The AuNPs enable the detection of dimethyl sulfide and histamine at limits of 0.5 and 0.03

16 o important volatile biogenic markers, i.e., dimethyl sulfide and histamine, is developed to monitor

17 depletion, as well as the rapid oxidation of dimethyl sulfide and mercury in the Antarctic boundary l

18 substitutions with the neutral nucleophiles dimethyl sulfide and triethylamine and the bromination w

19 by biotin or the nonphysiological products, dimethyl sulfide and trimethylamine.

20 ions are reactive toward dimethyl disulfide, dimethyl sulfide, and allyl iodide and most toward water

21 s affected by time include 2-methylpropanal, dimethyl sulfide, and benzaldehyde.

22 reased hydrogen sulfide (H2S), methanethiol, dimethyl sulfide, and carbon disulfide concentrations.

23 o coordinate various ligands like imidazole, dimethyl sulfide, and carbon monoxide depending on the r

24 oprene (C(5)H(8)), methyl bromide (CH(3)Br), dimethyl sulfide, and oxygen (O(2)), which increased sub

25 itrite to a water-soluble phosphine (tppts), dimethyl sulfide, and the biological thiols cysteine (Cy

26 Both the alternate substrate, dimethyl sulfide, and the competitive product inhibitor,

27 Significant amounts of dimethyl sulfide are emitted from cruciferous vegetables

28 hat procellariiform seabird species that use dimethyl sulfide as a foraging cue selectively forage on

29 controlled to release increasing amounts of dimethyl sulfide as the supply of DMSP exceeds cellular

30 iisobutylaluminum hydride (DIBAL) and borane dimethyl sulfide (BMS) has shown great potential in redu

31 tron ionization (EI) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3

32 riethylsilane, cycloheptatriene, or a borane-dimethyl sulfide complex.

33 chemoselective reductive-opening by a borane-dimethyl sulfide complex.

34 obial nitrate reductase, selenate reductase, dimethyl sulfide dehydrogenase, ethylbenzene dehydrogena

35 l)-R-pyridinium) with dimethylplatinum-micro-dimethyl sulfide dimer.

36 sulfur compounds detected were methanethiol, dimethyl sulfide, dimethyl disulfide, and dimethyl trisu

37 parts per trillion for select VOCs including dimethyl sulfide, dimethylamine, and trimethylamine.

38 sulfoniopropionate (DMSP) cleavage, yielding dimethyl sulfide (DMS) and acrylate, provides vital carb

39 ination with the algal-derived infochemicals dimethyl sulfide (DMS) and dimethylsulfoniopropionate (D

40 reactivity with aldehydes and the effects of dimethyl sulfide (DMS) and Saharan dust on aerosol pH; a

41 sulfoniopropionate (DMSP) and its catabolite dimethyl sulfide (DMS) are key marine nutrients(1,2) tha

42 kite heterojunction formation by introducing dimethyl sulfide (DMS) as a soft Lewis base additive in

43 ide to form water oxide and the oxidation of dimethyl sulfide (DMS) by hydrogen peroxide to form dime

44 Dimethyl sulfide (DMS) contributes significantly to the

45 Oceanic emissions of dimethyl sulfide (DMS) have long been known to influence

46 ay involving dimethyl sulfoxide (DMSO), with dimethyl sulfide (DMS) identified as the reduction produ

47 Dimethyl sulfide (DMS) is a key compound in global sulfu

48 Ocean-emitted dimethyl sulfide (DMS) is a major source of climate-cool

49 As dimethyl sulfide (DMS) is a reliable marker for meat fre

50 Dimethyl sulfide (DMS) is produced in large quantities a

51 Oceanic dimethyl sulfide (DMS) is the largest natural source of

52 laboratory measurements of alpha-pinene and dimethyl sulfide (DMS) oxidation systems, we characteriz

53 The production of the marine trace gas dimethyl sulfide (DMS) provides 90% of the marine biogen

54 nic acid (MSA) formation in the oxidation of dimethyl sulfide (DMS) remains unclear.

55 Oceanic emissions of volatile dimethyl sulfide (DMS) represent the largest natural sou

56 Marine emissions of dimethyl sulfide (DMS) to the atmosphere play a fundamen

57 tal thiols, S-methyl-l-methionine (SMM), and dimethyl sulfide (DMS) were analysed periodically.

58 methanethiol (MeSH), ethanethiol (EtSH), and dimethyl sulfide (DMS) were assessed in wines post-bottl

59 P lyases cleave DMSP, producing acrylate and dimethyl sulfide (DMS), a climate-active gas with roles

60 The presence of dimethyl sulfide (DMS), either as a component originatin

61 Dimethyl sulfide (DMS), emitted from the oceans, is the

62 e conversion of dimethyl sulfoxide (DMSO) to dimethyl sulfide (DMS), reversibly, in the presence of s

63 Oceans dominate emissions of dimethyl sulfide (DMS), the major natural sulfur source.

64 ntermediates in the atmospheric oxidation of dimethyl sulfide (DMS), was generated by flash pyrolysis

65 BlMGL) produced the sulfur volatile compound dimethyl sulfide (DMS).

66 sms(2,3) and the major precursor for gaseous dimethyl sulfide (DMS).

67 the marine volatile organic sulfur compound dimethyl sulfide (DMS).

68 Dimethyl sulfide (DMS; CH(3)SCH(3)), a biogenically prod

69 nism by which anthropogenic SO(2) and marine dimethyl sulfide emissions generate secondary biogenic a

70 terised by a high level of sulfur compounds (dimethyl sulfide, ethanethiol), and ester and alcohol co

71 While transgenic lines emitted dimethyl sulfide from leaves and roots, no sulfur-contai

72 the olefin followed by brief treatment with dimethyl sulfide gave a mixture of diastereomeric ozonid

73 none 12c in CH2Cl2 and reductive workup with dimethyl sulfide generated unstable beta-formyl ester 21

74 ived metabolites, including volatile esters, dimethyl sulfide, glycerol and mannoproteins with harves

75 Dimethyl sulfide has been studied in the context of glob

76 m the solvolysis data, the nucleofugality of dimethyl sulfide in different proportions of this ionic

77 ules of keystone significance: saxitoxin and dimethyl sulfide in marine communities and tetrodotoxin

78 Furthermore, DMSO was converted to dimethyl sulfide in situ, which served as the methylthio

79 lent yield and enantiomeric excess by borane-dimethyl sulfide in the presence of a chiral oxazaboroli

80 e that the ability of DMSOR to be reduced by dimethyl sulfide is lost upon mutation of Tyr-114 and th

81 own to arise on extended aerobic exposure to dimethyl sulfide, is susceptible to a further degradativ

82 y a compensatory (100-fold) up-regulation in dimethyl sulfide metabolic enzymes.

83 We identified carbon disulfide, dimethyl sulfide, methionol and benzothiazole as key sul

84 y, the release of acetone, carbon disulfide, dimethyl sulfide, nitromethane, pentane, 3-methylfuran,

85 um carbonate precipitation and production of dimethyl sulfide, often blooms in mid-latitude at the be

86 usly shunts as much as 59% of DMSP uptake to dimethyl sulfide production.

87 ted with tailpipe emissions of formaldehyde, dimethyl sulfide, propene, and methyl ketene.

88 reaction in which the accumulating product, dimethyl sulfide, reacts with oxidized enzyme to yield t

89 our results, we postulate a heme-based redox/dimethyl sulfide sensory function of MA4561 and propose

90 xothermic reactions (ca. 50 kcal mol(-1) for dimethyl sulfide) that can fragment or be stabilized via

91 , converting phosphines to phosphine oxides, dimethyl sulfide to dimethyl sulfoxide, and dibenzylamin

92 Further, the nucleofugality of dimethyl sulfide was determined in mixtures containing h

93 The nucleofugality of dimethyl sulfide was measured in solvent mixtures contai

94 uch faster than the corresponding adducts of dimethyl sulfide, which are currently used extensively.

95 hanol with H(3)O(+), acetone with NO(+), and dimethyl sulfide with O(2)(+*) reagent ions in single br