ライフサイエンスコーパス: carbon-carbon double bond

1 installed at a site remote from the original carbon-carbon double bond).

2 egioselective oxygen radical addition to the carbon-carbon double bond.

3 the direct addition of sulfonyl anions to a carbon-carbon double bond.

4 se of the fact that EPA contains an addition carbon-carbon double bond.

5 lar exchange parameter, J, is modulated by a carbon-carbon double bond.

6 rins linked by a flexible chain containing a carbon-carbon double bond.

7 uring insertion of a Cu(I) -phosphido into a carbon-carbon double bond.

8 pids, which differ only by the geometry of a carbon-carbon double bond.

9 ) and cyanovinylene units linked entirely by carbon-carbon double bonds.

10 such as those differing in the positions of carbon-carbon double bonds.

11 rporate functional groups distal to existing carbon-carbon double bonds.

12 Unsaturated lipids contain one or multiple carbon-carbon double bonds.

13 ed ansa metallocenes are rare and limited to carbon-carbon double bonds.

14 heterogeneous catalysts capable of oxidizing carbon-carbon double bonds.

15 saturation or geometric configuration of the carbon-carbon double bonds.

16 through cleavage of the fatty acid tails at carbon-carbon double bonds.

17 esis is a powerful tool for the formation of carbon-carbon double bonds.

18 dditions of oxygen-hydrogen bonds across the carbon-carbon double bonds.

19 ling polymers via dynamic exchange of strong carbon-carbon double bonds.

20 n allows the direct formation of ethers from carbon-carbon double bonds.

21 ivatives, as well as amides bearing isolated carbon-carbon double bonds.

22 rn reacting with A2E to generate epoxides at carbon-carbon double bonds.

23 t attack carbon-nitrogen, carbon-sulfur, and carbon-carbon double bonds.

24 electivity with alcohols containing internal carbon-carbon double bonds.

25 the addition of water to isolated fatty acid carbon-carbon double bonds.

26 ynthetic procedure for the hydroamidation of carbon-carbon double bonds.

27 alytes specified by total acyl carbons:total carbon-carbon double bonds, 36:6, 36:5, and 34:3 PC and

28 iate, (4) acylpalladation of the neighboring carbon-carbon double bond, (5) reversible palladium beta

29 of the nitrogen-hydrogen bond to the pendent carbon-carbon double bond, affording the corresponding c

30 s from any monomers or polymers that contain carbon-carbon double bonds amenable to radical polymeriz

31 se at 1298 and 1250 cm(-1) are indicative of carbon--carbon double bonds and carbon--carbon single bo

32 his new DBO, ETX1317, contains an endocyclic carbon-carbon double bond and a fluoroacetate activating

33 ite energetically difficult protonation of a carbon-carbon double bond and also affecting inhibitory

34 iated by hydroxyl (OH) radical addition to a carbon-carbon double bond and apparently propagated thro

35 inyl units were inserted between the central carbon-carbon double bond and each of the reaction cente

36 ick reactions: the azidosulfenylation of the carbon-carbon double bond and the copper-catalyzed azide

37 Owing to the presence of two active carbon-carbon double bonds and a lactone unit, EVP serve

38 a component of human skin oil, contains six carbon-carbon double bonds and is very reactive with ozo

39 omers that differ only in the location(s) of carbon-carbon double bonds and/or the relative position

40 The pH-rate profiles for carbon-carbon double-bond and ketone reduction catalyzed

41 itutes an alpha,beta-difuctionalisation of a carbon-carbon double bond, and proceeds under mild condi

42 g in the location or (cis/trans) geometry of carbon-carbon double bonds are often incompletely separa

43 ring electron-rich, -neutral, and -deficient carbon-carbon double bonds are viable substrates for [3

44 nol tautomers, bearing OH groups adjacent to carbon-carbon double bonds, are not included in standard

45 However, the efficacy of the carbon-carbon double bond as an exchange coupler is dete

46 he presence of secondary carbinol groups and carbon-carbon double bonds, as in enzymatic reactions.

47 uent HOCl uptake occurs until all six of its carbon-carbon double bonds become chlorinated within 1-2

48 arge transport correlates with the number of carbon-carbon double bonds, but not with the extent of c

49 The oxygenation of carbon-carbon double bonds by iron enzymes generally res

50 antitation of unsaturated FAs with confident carbon-carbon double bond (C horizontal lineC) location

51 Visualizing the differential distribution of carbon-carbon double bond (C=C db) positional isomers of

52 The carbon-carbon double bond (C=C) conjugation length of ca

53 ity, largely because of the isomerism of the carbon-carbon double bond (C=C) in terms of its position

54 the detection of fatty acids (FA) and their carbon-carbon double bond (C=C) positional isomers in bi

55 Identifying carbon-carbon double bond (C=C) positions in complex lip

56 Covalent organic frameworks linked by carbon-carbon double bonds (C=C COFs) are an emerging cl

57 Repair of the carbon-carbon double bonds (C=C) in the CPD is initiated

58 of lipids but the effective localization of carbon-carbon double bonds (C=C) in unsaturated lipids t

59 r acyl chain configurations and locations of carbon-carbon double bonds (C=C) remains challenging due

60 Carbon-carbon double-bond (C=C) positions are also local

61 re activated and tested for the promotion of carbon-carbon double-bond cis-trans isomerization reacti

62 itor (two hydroxamates that only differ by a carbon-carbon double bond) complexes of human fibroblast

63 it has a twist angle of 45.2 degrees for the carbon-carbon double bond connecting the two bifluorenyl

64 l amination of substrates containing several carbon-carbon double bonds could be achieved, demonstrat

65 involving electron-withdrawing groups on the carbon--carbon double bond (e.g., -CN, -CHO, and -NO(2))

66 est that alkenones with different numbers of carbon-carbon double bonds express significantly differe

67 ntrolled addition of diazomethyl radicals to carbon-carbon double bonds followed by intramolecular ri

68 observed unidirectional isomerization of the carbon-carbon double bonds from all cis to all trans and

69 that differ in (i) the location of a single carbon-carbon double bond, (ii) the stereochemistry of t

70 The reduction of the carbon-carbon double bond in an alpha,beta-unsaturated k

71 ed by type I IDI involves protonation of the carbon-carbon double bond in IPP or DMAPP to form a tert

72 ty of allylic isoprenoid diphosphates to the carbon-carbon double bond in isopentenyl diphosphate (IP

73 Da mass difference indicated localization of carbon-carbon double bond in MS/MS spectra.

74 ind to a group of cyclodextrin dimers with a carbon-carbon double bond in the linker.

75 workflow was finally applied for pinpointing carbon-carbon double bonds in 77 polar lipids from an ye

76 -regulated antioxidative enzyme that reduces carbon-carbon double bonds in a variety of alpha, beta-u

77 for the first time for the determination of carbon-carbon double bonds in fatty acyl chains using hi

78 was employed for the first time to pinpoint carbon-carbon double bonds in free and conjugated fatty

79 and widely adopted strategy for constructing carbon-carbon double bonds in organic chemistry.

80 n-1 and sn-2 positions, and the positions of carbon-carbon double bonds in the lipid acyl chains.

81 e effects of various single and multiple cis carbon-carbon double bonds in the sn-2 acyl chains of na

82 the enyne-carbodiimides 7 having the central carbon-carbon double bond incorporated as part of the cy

83 Michael addition of methanol to the carbon-carbon double bond initiated the consecutive form

84 Hydroamidation of carbon-carbon double bonds is an attractive strategy for

85 hat fatty acid unsaturation (i.e., number of carbon-carbon double bonds) is fundamentally constrained

86 ddition of a silicon hydride (Si-H) across a carbon-carbon double bond, is one of the largest-scale i

87 While metathesis reactions involving carbon-carbon double bonds, namely olefin metathesis, ha

88 non-heme iron center to oxidatively cleave a carbon-carbon double bond of a carotenoid substrate.

89 at is known to catalyze the reduction of the carbon-carbon double bond of alpha,beta-unsaturated alde

90 the leaving group ability of the former, the carbon-carbon double bond of imidazol-2-ylidenes can be

91 It is also possible for the carbon-carbon double bond of noroxomaritidine to be redu

92 the barrierless addition of dicarbon to the carbon-carbon double bond of the 2-methyl-1,3-butadiene

93 , (2) carbopalladation of the least hindered carbon-carbon double bond of the diene, (3) palladium mi

94 ddition of one aromatic phenol carbon to the carbon-carbon double bond of the epoxyalkenal.

95 by an addition of the phenyl radical to the carbon-carbon double bond of the ethylene molecule formi

96 ide-N-oxyl (PINO) radical, which adds to the carbon-carbon double bond of vinyl arenes and recombines

97 transfer reactions involving insertions into carbon-carbon double bonds of alkenes and styrenes or be

98 The carbon-carbon double bonds of NAS modified QDs polymeriz

99 olesterol reductase (DHCR24) reduce specific carbon-carbon double bonds of the sterol moiety using a

100 containing these residues, as well as at the carbon-carbon double bonds of unsaturated phospholipids.

101 ra that permit (i) unambiguous assignment of carbon-carbon double bond position(s) and (ii) relative

102 egiochemistry along the glycerol backbone or carbon-carbon double bond position(s) in unsaturated fat

103 f the GPL headgroup, fatty acyl composition, carbon-carbon double bond position(s) in unsaturated fat

104 ity separation allowed identification of the carbon-carbon double-bond position and sn-position, enab

105 A simple, fast approach elucidated carbon-carbon double bond positions in unsaturated lipid

106 inor structural differences such as relative carbon-carbon double bond positions were found in severa

107 Di-, tri-, and tetrasubstituted carbon-carbon double bonds react with similar efficiency

108 tal structure of a mammalian steroid hormone carbon-carbon double bond reductase, human Delta(4)-3-ke

109 maritinamine from noroxomaritidine through a carbon-carbon double bond reduction.

110 -thioesters to introduce E- and Z-configured carbon-carbon double bonds, respectively.

111 Olefins containing single or multiple carbon-carbon double bonds serve as vital intermediates

112 alkyl and aryl esters, amide, cyano, and the carbon-carbon double bond survive the reaction.

113 tions based on the proximity of each steroid carbon-carbon double bond to the re-face of the nicotina

114 that reflects divergent trajectories of the carbon-carbon double bond to the reacting carbene center

115 hat involves the reduction of the alpha,beta-carbon=carbon double bond to a single bond.

116 The surface linker, with an active carbon-carbon double bond, was preimmobilized on the gol

117 n at the carbinol position, phenyl ring, and carbon-carbon double bond were all found to have signifi

118 Carbon-carbon double bonds were identified in the conden

119 dalities, and in all cases, the positions of carbon-carbon double bonds were unequivocally assigned b

120 ially when it comes to the regiochemistry of carbon-carbon double bonds, which play a major role in d

121 lysis of oleic acid, and localization of the carbon-carbon double bond within a lysophosphatidic acid

122 v, HOCl forms chlorohydrins by adding across carbon-carbon double bonds without breaking the carbon b