ライフサイエンスコーパス: decane

1 ophenylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decane ].

2 lein in squalene) to 54 A (monoeicosenoin in decane).

3 hexene, and 1-hexene have been determined in decane.

4 ch lattice oxide ions abstract hydrogen from decane.

5 of oxidative cleavage varies from methane to decane.

6 ar organic liquids such as cyclohexane and n-decane.

7 e membrane-thickening agents cholesterol and decane.

8 nces between rate constants for ethane and n-decane (~10(8)) reflect an increase in the entropy of ga

9 tuted RRA, threo(trans)-1-aza-5-phenyl[4.4.0]decane (12a), was equipotent to unconstrained threo-MP a

10 found in 3,9-diaza-3,9-dimethylbicyclo[4.4.0]decane-2,10-dione (7).

11 rivative, 3,9-diaza-3,9-dioctylbicyclo[4.4.0]decane-2,10-dione (8), was prepared, and solvent extract

12 )phenyl-5-oxopen tyl)]-1,3,8-triazaspiro[4.5]decane-2,4-dione hydrochloride (RS 102221) (0.05-0.5 mic

13 o) phenyl-5-oxopentyl]1,3,8-triazaspiro[4.5] decane-2,4-dione hydrochloride (RS102221) and 1,2,3, 4,1

14 The discovery of 1,3,8-triazaspiro[4.5]decane-2,4-diones (spirohydantoins) as a structural clas

15 1,3,8-Triazaspiro[4.5]decane-2,4-diones (spirohydantoins) were optimized as an

16 e (N-N-diethyl-8,8-dipropyl-2-azaspiro [4.5] decane-2-propanamine; trade name, Atiprimod) is an orall

17 0(3,7)]decane-2beta-carboxylic acid methyl ester (5a) is a sele

18 hienylmethylene)-7-azatricyclo[4.3.1.0(3, 7)]decane-2beta-carboxylic acid methyl ester (5h) exhibits

19 methyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-3-acetic acid, methyl ester] are G protein-biased

20 yphenyl)-1-piperazinyl]ethyl]-8-azaspiro[4.5]decane-7, 9-dione (BMY 7378).

21 yphenyl)piperazin-1-yl)ethyl]-8-azaspiro[4,5]decane-7,9-d ione (BMY 7378), despite the ability to det

22 enzyl)-N-(4-methylbenzyl)-2,7-diazaspiro(4.5)decane-7-carboxa mide inhibits both the kinase and RNase

23 enzyl)-N-(4-methylbenzyl)-2,7-diazaspiro(4.5)decane-7-carboxa mide, a novel, IRE1alpha-selective kina

24 For longer alkanes such as n-decane, a single guest enters and the aromatic walls of

25 Relative responses of n-decane, an unlabeled internal standard otherwise absent

26 High boiling point compounds such as n-decane and 2,2-dimethylpropylbenzene were not completely

27 The new 2-azatetracyclo[4.4.0.0.(4,9)0(7,10)]decane and 3-azatetracyclo[6.1.1.0.(2,7)0(5,9)]decane st

28 e of reaction of [(dippe)NiH]2 with 2M3BN in decane and N,N-dimethylformamide (DMF) allowed for the c

29 In the case of n-decane and n-dodecane, the resulting alkylarenes are exc

30 w surface tension, including alkanes such as decane and octane.

31 enzymatic final measurement was performed in decane and using tert-butylhydroperoxide as substrate of

32 rface between an apolar hydrophobic phase (n-decane) and an aqueous phase mimics the biological pathw

33 a range of stereodefined fused bicyclo[4.4.0]decanes are accessible, including those that contain aro

34 catalytic amount of Cu(ClO4)2.6H2O, TBHP in decane as an oxidant, and 1,10-phenanthroline as a ligan

35 ented to give 3,9-diazatricyclo[5.3.0.0(1,5)]decanes as conformationally restricted bis-pyrrolidines.

36 tion of cis and trans-fused oxabicyclo[4,4,0]decanes as products with the latter being strongly indic

37 W hydride (TON = 650) in the metathesis of n-decane at 150 degrees C.

38 BCPs composed of decane-based side chains and either triethyleneglycol- o

39 KvAP function in two different phospholipid decane bilayers is developed.

40 opogenic (naphthalene, tricyclo[5.2.1.0(2,6)]decane), biomass burning (guaiacol), and biogenic (alpha

41 s in 1,10-bis[p-(benzylammoniomethyl)phenoxy]decane bis(hexafluorophosphate) (A10A) were shown to beh

42 oxolane-linked gA dimer "inactivated" in GMO/decane but not in squalene-containing bilayers.

43 for assembling the azatricyclo[4.4.0.0(2,8)]decane core of gelsemine is described.

44 olinone alkaloids possessing a bicyclo[4.3.1]decane core, we report herein concise asymmetric total s

45 er of rates: C(6)D(6) > mesitylene-d(12) > n-decane-d(22) >> cyclohexane-d(12).

46 olvent (octadecene (ODE), n-nonane-d20, or n-decane-d22), affording ME nanocrystals, tri-n-butylphosp

47 s have been converted to either azaspiro[4.5]decane derivatives or functionalized tetrahydroisoquinol

48 with silver(I) salts and into 1-azaspiro[4.5]decane derivatives with gold(I) complexes.

49 ane (GMO) and diphytanoylphosphatidylcholine/decane (DiPhPC) bilayers.

50 -xylene, 2,2,4-trimethylpentane (isooctane), decane, dodecane, tetradecane, hexadecane, and 2,6,10,14

51 that kerogen suppresses the boiling point of decane due to the effect of confinement.

52 ere observed on spin-coated poly(bisphenol A decane ether) (BA-C10) films prepared with chloroform an

53 channels were measured in glycerylmonooleate/decane (GMO) and diphytanoylphosphatidylcholine/decane (

54 (see picture; yellow) and soft templates (n-decane; green).

55 The hydroniums in direct contact with n-decane have a reduced mobility.

56 ve ab initio simulations on the same water/n-decane interface reproduced the experimentally derived f

57 ed ring of unsaturated tricyclo[5.3.0.0(2,6)]decane intermediates (perhaps the result of 10-electron

58 Adding an oil, i.e., decane, into a CTAB-EtOH-TEOS ammonia solution leads to

59 ion of product molecular weights, in which n-decane is the predominant high-molecular-weight product

60 An internal standard, decane, is present in the organic extracting solvent, an

61 n-heptadecane (n-C17), tricyclo[5.2.1.0(2,6)]decane (JP-10), and vapors of diesel fuel and Southern L

62 des were obtained by painting a phospholipid:decane mixture across a cylindrical pore etched into a 2

63 charged azepanyl or 1,4-dioxa-8-azaspiro[4.5]decane moiety at position 3.

64 cess to highly functionalized 2-azaspiro[4.5]decanes, morphan compounds, and the azatricyclic core of

65 SOA precursors were n-decane (n-C10), n-pentadecane (n-C15), n-heptadecane (n-

66 ( n-hexane, n-heptane, n-octane, n-nonane, n-decane, n-undecane, and n-dodecane) in blood using heads

67 onane ring embedded within the bicyclo[5.2.1]decane-N,O-acetal moiety of sieboldine A was a formidabl

68 During the aerobic gas-phase conversion of n-decane over iron molybdate, the product distribution cor

69 med silica, or zeolite seed), and many oils (decane, petroleum ether, or ethyl acetate).

70 Decane played two roles: (a) as a pore expansion agent (

71 hreo-1-aza-3 or 4-substituted-5-phenyl[4.4.0]decanes (quinolizidines), which were envisioned as restr

72 quantification limits for n-hexane through n-decane ranged from 0.069 to 0.132 ng/mL.

73 tion structures for 10-R-9-borabicyclo[3.3.2]decane reagents.

74 The 10-R group and borabicyclo[3.3.2]decane ring conformation effects were analyzed to unders

75 of the groups on the core 1-azabicyclo[5.3.0]decane ring system by a [3,3] sigmatropic rearrangement

76 clo[3.3.1.1 approximately 3,7 approximately ]decane ring system is described.

77 nces of the newly formed benzo bicyclo[3.3.2]decane ring system.

78 ged bicyclo[5.3.1]undecane and bicyclo[4.3.1]decane ring systems.

79 c piperidine-pyrrolidine (2,8-diazaspiro[4.5]decane) ring systems was developed.

80 we have utilized a novel 2,8-diazaspiro[4.5]decane scaffold as a template.

81 novel and facile access to the bicyclo[5.3.0]decane skeleton from simple and readily available compon

82 The bicyclo[5.3.0]decane skeleton is one of the most commonly encountered

83 nditions followed by introduction of a 5.5 M decane solution of tert-butyl hydroperoxide (TBHP) to ge

84 (2)(CO)(10) and 3,5-Me(2)BT with UV light in decane solution under an atmosphere of H(2) produces com

85 king place intrinsically or extrinsically to decane solvent cage assemblies.

86 activation enthalpies going from pentane to decane solvent, suggesting that enthalpy-entropy compens

87 cane and 3-azatetracyclo[6.1.1.0.(2,7)0(5,9)]decane structures formed in the photochemical reactions

88 rocarbon, stearic acid, added to the ambient decane synergistically enhance the effect and lead to wa

89 tathesis to build the bridging bicyclo[4.3.1]decane terpene framework.

90 sed to analyze the thermodynamic behavior of decane that was sorbed in the kerogen and show that kero

91 In GMO/decane (thick) bilayers, the largest flicker frequency o

92 Pairwise interactions between n-alkanes from decane to octadecane in water have been studied by singl

93 addition of 20 or 40 mol % cholesterol or n-decane to the liposome preparation.

94 Cs (2-methylheptane, styrene, propylbenzene, decane, undecane) at conditions simulating human breath,

95 ently assembles the azatricyclo[4.4.0.0(2,8)]decane unit of gelsemine.

96 The swelling behavior of this kerogen with decane was analyzed using traditional test-tube swelling

97 sotwistane (2,8-dibromotricyclo[4.3.1.0(3,7)]decane) was inadvertently formed.

98 ed arylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decanes, were prepared, and their abilities to inhibit h

99 iarylylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decanes, were synthesized and evaluated for their abilit

100 l-1-yl)borate; L = 1-S(acetyl)tris(pyrazolyl)decane], were covalently linked onto the electrodes form

101 clo[2.2.1]heptane and 1,6-diazabicyclo[4.3.1]decane, which each have two expected contributing struct