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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 Carbon-carbon double bonds were identified in the conden

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

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