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1 ophenylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decane ].
2 lein in squalene) to 54 A (monoeicosenoin in decane).
3 on to afford congeners of 7-azabicyclo[4.3.1]decane.
4 alloy for selective propylene synthesis from decane.
5 ch lattice oxide ions abstract hydrogen from decane.
6 of oxidative cleavage varies from methane to decane.
7 hexene, and 1-hexene have been determined in decane.
8 ar organic liquids such as cyclohexane and n-decane.
9 e membrane-thickening agents cholesterol and decane.
10 nces between rate constants for ethane and n-decane (~10(8)) reflect an increase in the entropy of ga
11 tuted RRA, threo(trans)-1-aza-5-phenyl[4.4.0]decane (12a), was equipotent to unconstrained threo-MP a
12 found in 3,9-diaza-3,9-dimethylbicyclo[4.4.0]decane-2,10-dione (7).
13 rivative, 3,9-diaza-3,9-dioctylbicyclo[4.4.0]decane-2,10-dione (8), was prepared, and solvent extract
14 )phenyl-5-oxopen tyl)]-1,3,8-triazaspiro[4.5]decane-2,4-dione hydrochloride (RS 102221) (0.05-0.5 mic
15 o) phenyl-5-oxopentyl]1,3,8-triazaspiro[4.5] decane-2,4-dione hydrochloride (RS102221) and 1,2,3, 4,1
16       The discovery of 1,3,8-triazaspiro[4.5]decane-2,4-diones (spirohydantoins) as a structural clas
17                        1,3,8-Triazaspiro[4.5]decane-2,4-diones (spirohydantoins) were optimized as an
18 e (N-N-diethyl-8,8-dipropyl-2-azaspiro [4.5] decane-2-propanamine; trade name, Atiprimod) is an orall
19                                       0(3,7)]decane-2beta-carboxylic acid methyl ester (5a) is a sele
20 hienylmethylene)-7-azatricyclo[4.3.1.0(3, 7)]decane-2beta-carboxylic acid methyl ester (5h) exhibits
21 methyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-3-acetic acid, methyl ester] are G protein-biased
22 ]nonane-3-carboxylate and (S)-2-azaspiro[4,5]decane-3-carboxylate have favorable characteristics.
23 lkyl)-1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane 5 were successfully synthesized for the first tim
24 yphenyl)-1-piperazinyl]ethyl]-8-azaspiro[4.5]decane-7, 9-dione (BMY 7378).
25 yphenyl)piperazin-1-yl)ethyl]-8-azaspiro[4,5]decane-7,9-d ione (BMY 7378), despite the ability to det
26 enzyl)-N-(4-methylbenzyl)-2,7-diazaspiro(4.5)decane-7-carboxa mide inhibits both the kinase and RNase
27 enzyl)-N-(4-methylbenzyl)-2,7-diazaspiro(4.5)decane-7-carboxa mide, a novel, IRE1alpha-selective kina
28                 For longer alkanes such as n-decane, a single guest enters and the aromatic walls of
29 ) electrolyte to facilely upgrade alkanes (n-decane), alkenes (1-decene), and CO(2) feedstocks.
30                      Relative responses of n-decane, an unlabeled internal standard otherwise absent
31       High boiling point compounds such as n-decane and 2,2-dimethylpropylbenzene were not completely
32 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
33  construction of 10-deoxy-1,6-dioxaspiro[4.5]decane and 4-deoxy-6,8-dioxabicyclo[3.2.1]octane framewo
34 e of reaction of [(dippe)NiH]2 with 2M3BN in decane and N,N-dimethylformamide (DMF) allowed for the c
35                             In the case of n-decane and n-dodecane, the resulting alkylarenes are exc
36 g aliphatic compounds, the strain degraded n-decane and n-hexadecane as the sole sources of carbon at
37 w surface tension, including alkanes such as decane and octane.
38  identified a novel VOC signature comprising decane and other long-chain alkane compounds that is ind
39 d using the volatile (14)C-labeled chemicals decane and tetralin.
40 enzymatic final measurement was performed in decane and using tert-butylhydroperoxide as substrate of
41 rface between an apolar hydrophobic phase (n-decane) and an aqueous phase mimics the biological pathw
42 in 273 grown with 1,10-difluorodecane (DFD), decane, and acetate were performed.
43 B-2 were significantly more abundant in both decane- and DFD-grown cells compared to acetate-grown ce
44 entative PFAS, and trichloroethene (TCE) and decane are used as representative NAPLs.
45 a range of stereodefined fused bicyclo[4.4.0]decanes are accessible, including those that contain aro
46  catalytic amount of Cu(ClO4)2.6H2O, TBHP in decane as an oxidant, and 1,10-phenanthroline as a ligan
47 ented to give 3,9-diazatricyclo[5.3.0.0(1,5)]decanes as conformationally restricted bis-pyrrolidines.
48 tion of cis and trans-fused oxabicyclo[4,4,0]decanes as products with the latter being strongly indic
49 W hydride (TON = 650) in the metathesis of n-decane at 150 degrees C.
50                             BCPs composed of decane-based side chains and either triethyleneglycol- o
51  KvAP function in two different phospholipid decane bilayers is developed.
52 opogenic (naphthalene, tricyclo[5.2.1.0(2,6)]decane), biomass burning (guaiacol), and biogenic (alpha
53 s in 1,10-bis[p-(benzylammoniomethyl)phenoxy]decane bis(hexafluorophosphate) (A10A) were shown to beh
54 oxolane-linked gA dimer "inactivated" in GMO/decane but not in squalene-containing bilayers.
55 ydrophobic surfaces, water-toluene and water-decane, by surface-sensitive nonlinear spectroscopy and
56             Here, we report the detection of decane (C(10)H(22)), undecane (C(11)H(24)), and dodecane
57  for assembling the azatricyclo[4.4.0.0(2,8)]decane core of gelsemine is described.
58 g the synthetically challenging oxaspiro[4,5]decane core of numerous medicinal agents, agrochemicals,
59        The unique 9-azatricyclo[4.3.1.0(3,8)]decane core was assembled through an efficient domino se
60 olinone alkaloids possessing a bicyclo[4.3.1]decane core, we report herein concise asymmetric total s
61 er of rates: C(6)D(6) > mesitylene-d(12) > n-decane-d(22) >> cyclohexane-d(12).
62 olvent (octadecene (ODE), n-nonane-d20, or n-decane-d22), affording ME nanocrystals, tri-n-butylphosp
63 en 40 was included in the formulation, using decane/decanol/dodecanol as coporogens.
64 s have been converted to either azaspiro[4.5]decane derivatives or functionalized tetrahydroisoquinol
65 with silver(I) salts and into 1-azaspiro[4.5]decane derivatives with gold(I) complexes.
66 ane (GMO) and diphytanoylphosphatidylcholine/decane (DiPhPC) bilayers.
67  C) was performed in three alkane solutions, decane, dodecane, and hexadecane.
68 -xylene, 2,2,4-trimethylpentane (isooctane), decane, dodecane, tetradecane, hexadecane, and 2,6,10,14
69 that kerogen suppresses the boiling point of decane due to the effect of confinement.
70 ere observed on spin-coated poly(bisphenol A decane ether) (BA-C10) films prepared with chloroform an
71  unusual triterpenes bearing a bicyclo[4.3.1]decane fragment (22).
72 ts the signature tricyclo[3.3.1(2,10).1(1,4)]decane framework characteristic of phragmalin natural pr
73 channels were measured in glycerylmonooleate/decane (GMO) and diphytanoylphosphatidylcholine/decane (
74  (see picture; yellow) and soft templates (n-decane; green).
75      The hydroniums in direct contact with n-decane have a reduced mobility.
76 er examines the flow of hexane, heptane, and decane in carbon nanotubes (CNTs) of pore diameters 1-8
77 mportant gamma-ketoamides and 2-Azaspiro[4.5]decanes in one pot in good to excellent yields.
78 er to a mixture of an ionic surfactant and n-decane induces aperiodic ordering of oil-swollen spheric
79 ve ab initio simulations on the same water/n-decane interface reproduced the experimentally derived f
80 n for SCN(-) to both water-toluene and water-decane interfaces is driven by an increase in entropy, w
81 ed ring of unsaturated tricyclo[5.3.0.0(2,6)]decane intermediates (perhaps the result of 10-electron
82                         Adding an oil, i.e., decane, into a CTAB-EtOH-TEOS ammonia solution leads to
83 ion of product molecular weights, in which n-decane is the predominant high-molecular-weight product
84                        An internal standard, decane, is present in the organic extracting solvent, an
85 n-heptadecane (n-C17), tricyclo[5.2.1.0(2,6)]decane (JP-10), and vapors of diesel fuel and Southern L
86                                        Using decane microdroplets, we show that both EOF and hydrosta
87 des were obtained by painting a phospholipid:decane mixture across a cylindrical pore etched into a 2
88 charged azepanyl or 1,4-dioxa-8-azaspiro[4.5]decane moiety at position 3.
89 e interfacial layer, aligns precisely with a decane molecule, facilitating propylene production.
90 cess to highly functionalized 2-azaspiro[4.5]decanes, morphan compounds, and the azatricyclic core of
91                        SOA precursors were n-decane (n-C10), n-pentadecane (n-C15), n-heptadecane (n-
92  prepared with different oils (n-dodecane, n-decane, n-octane, soybean oil, olive oil, tricaprylin) o
93 ( n-hexane, n-heptane, n-octane, n-nonane, n-decane, n-undecane, and n-dodecane) in blood using heads
94 onane ring embedded within the bicyclo[5.2.1]decane-N,O-acetal moiety of sieboldine A was a formidabl
95 tially expressed during growth with acetate, decane, or DFD, suggesting the bacterium's biosynthetic
96 During the aerobic gas-phase conversion of n-decane over iron molybdate, the product distribution cor
97 med silica, or zeolite seed), and many oils (decane, petroleum ether, or ethyl acetate).
98                                              Decane played two roles: (a) as a pore expansion agent (
99 hreo-1-aza-3 or 4-substituted-5-phenyl[4.4.0]decanes (quinolizidines), which were envisioned as restr
100 quantification limits for n-hexane through n-decane ranged from 0.069 to 0.132 ng/mL.
101 tion structures for 10-R-9-borabicyclo[3.3.2]decane reagents.
102         The 10-R group and borabicyclo[3.3.2]decane ring conformation effects were analyzed to unders
103 of the groups on the core 1-azabicyclo[5.3.0]decane ring system by a [3,3] sigmatropic rearrangement
104 clo[3.3.1.1 approximately 3,7 approximately ]decane ring system is described.
105 nces of the newly formed benzo bicyclo[3.3.2]decane ring system.
106 ged bicyclo[5.3.1]undecane and bicyclo[4.3.1]decane ring systems.
107 c piperidine-pyrrolidine (2,8-diazaspiro[4.5]decane) ring systems was developed.
108  we have utilized a novel 2,8-diazaspiro[4.5]decane scaffold as a template.
109  a medicinally relevant 6-oxa-2-azaspiro[4.5]decane scaffold.
110 novel and facile access to the bicyclo[5.3.0]decane skeleton from simple and readily available compon
111                            The bicyclo[5.3.0]decane skeleton is one of the most commonly encountered
112  dynamics (MD) simulations, we investigate a decane-sodium dodecyl sulfate (SDS)-brine system, genera
113 nditions followed by introduction of a 5.5 M decane solution of tert-butyl hydroperoxide (TBHP) to ge
114 (2)(CO)(10) and 3,5-Me(2)BT with UV light in decane solution under an atmosphere of H(2) produces com
115 king place intrinsically or extrinsically to decane solvent cage assemblies.
116  activation enthalpies going from pentane to decane solvent, suggesting that enthalpy-entropy compens
117 cane and 3-azatetracyclo[6.1.1.0.(2,7)0(5,9)]decane structures formed in the photochemical reactions
118 rocarbon, stearic acid, added to the ambient decane synergistically enhance the effect and lead to wa
119 tathesis to build the bridging bicyclo[4.3.1]decane terpene framework.
120 sed to analyze the thermodynamic behavior of decane that was sorbed in the kerogen and show that kero
121                                       In GMO/decane (thick) bilayers, the largest flicker frequency o
122                                Addition of n-decane to mixtures of surfactant and water instead leads
123 Pairwise interactions between n-alkanes from decane to octadecane in water have been studied by singl
124  addition of 20 or 40 mol % cholesterol or n-decane to the liposome preparation.
125 Cs (2-methylheptane, styrene, propylbenzene, decane, undecane) at conditions simulating human breath,
126 ummary, elevated serum levels of the alkanes decane, undecane, and dodecane were associated with sPTB
127                                              Decane, undecane, and dodecane were significantly associ
128 ently assembles the azatricyclo[4.4.0.0(2,8)]decane unit of gelsemine.
129  assembled by synthesis of the bicyclo[4.3.1]decane via nitrile-oxide dipolar cycloaddition.
130 h for the synthesis of tricyclo[5.2.1.0(1,5)]decanes via radical cyclization was explored.
131   The swelling behavior of this kerogen with decane was analyzed using traditional test-tube swelling
132 sotwistane (2,8-dibromotricyclo[4.3.1.0(3,7)]decane) was inadvertently formed.
133 ed arylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decanes, were prepared, and their abilities to inhibit h
134 iarylylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decanes, were synthesized and evaluated for their abilit
135 l-1-yl)borate; L = 1-S(acetyl)tris(pyrazolyl)decane], were covalently linked onto the electrodes form
136 clo[2.2.1]heptane and 1,6-diazabicyclo[4.3.1]decane, which each have two expected contributing struct

 
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