ライフサイエンスコーパス: allyl alcohol

1 d a compound requiring metabolic activation (allyl alcohol).

2 ping of the quinonemethide intermediate with allyl alcohol.

3 trated using the example of the amination of allyl alcohol.

4 the C-H olefination reaction with olefin and allyl alcohol.

5 te a pericyclic group transfer reaction with allyl alcohols.

6 of N-ribofuranosylurea (1.6 x 10(-4) M) and allyl alcohol (0.14 M), indicating that the glycoside bo

7 The most striking were allyl alcohol (2700-fold), which likely needs to be meta

8 e of the acid-catalyzed ring opening of 3 to allyl alcohol 4 in a polar reaction medium and of the he

9 ons of 8-13, in the absence of phosphite, to allyl alcohol 7 and/or vinyl ether 5 were measured quant

10 n the amounts of product vinyl ether (5) and allyl alcohol (7) formed.

11 Orthoester Johnson-Claisen rearrangement of allyl alcohol (+)-9 (98% ee) in diisopropylethylamine fu

12 One scheme utilizes allyl alcohol, a compound that is not toxic to cells but

13 combining CCl(4) (centrilobular injury) with allyl alcohol (AA) (periportal injury), as well as in a

14 oly(dimethylsiloxane) (PDMS) membrane and an allyl alcohol (AA) membrane to the detection of methanol

15 s and several olefinic precursors, including allyl alcohol (AA), methyl vinyl ketone (MVK), 2-methyl-

16 tetrachloride [CCl4]) or periportal regions (allyl alcohol [AA]).

17 aining, and cell viability after exposure to allyl alcohol and acetaminophen demonstrated the in vitr

18 The rates of permanganate oxidation of allyl alcohol and acrylonitrile were determined, and the

19 Ratios of TOFs for hydrogenation of allyl alcohol and beta-methallyl alcohol are as high as

20 , the ratio of TOFs for the hydrogenation of allyl alcohol and crotyl alcohol is 39 with average part

21 sis of Barton PTOC esters in the presence of allyl alcohol and tert-butyl mercaptan undergo nucleophi

22 nds to periportal injury, such as induced by allyl alcohol and to choline-deficiency models of hepato

23 The products of the former are allyl alcohols (and, in some cases, dienes) and are keto

24 of 4-aryl-1,1,1-trifluorobut-3-en-2-ols [CF3-allyl alcohols, ArCH horizontal lineCHCH(OH)CF3] with ar

25 Allyl alcohols are obtained with a regio-preference for

26 r/acceptor carbenoids and highly substituted allyl alcohols are used as substrates.

27 benzamide and cinnamamide derivatives using allyl alcohol as a coupling partner catalyzed by Rh(III)

28 Specifically, using allyl alcohol as a tractable, inexpensive acrolein proel

29 The approach employs allyl alcohols as an efficient alternative to preactivat

30 ized 1,3-sultones were obtained by employing allyl alcohols as substrates.

31 y coordinating carbonyl-directed coupling of allyl alcohols at the C-4 position of indole derivatives

32 pargyl alcohol reduction intermediate having allyl alcohol bound as a ferracycle to FeMo-cofactor Fe6

33 h the HMBPP "parent" molecules, ethylene and allyl alcohol, bound to a nitrogenase FeMo cofactor.

34 e reaction between a racemic aldehyde and an allyl alcohol, catalyzed by using axially chiral iridium

35 es, such as 1-propanol, propionaldehyde, and allyl alcohol, compared to CORR alone.

36 endage point, hydrosilylation of a protected allyl alcohol followed by hydrosilylation of an enamide

37 In particular, our work shows that the allyl alcohols from beta-elimination are unlikely to und

38 se, is demonstrated to be able to oxidize an allyl alcohol group of eremophilanes into an alpha,beta-

39 sponse to periportal liver injury induced by allyl alcohol in rats.

40 to provide the corresponding functionalized allyl alcohols in good to excellent yields.

41 horizontal lineO) to yield the corresponding allyl alcohols in good yields.

42 LPCs) cloned from adult rat livers following allyl alcohol injury express hematopoietic stem cell and

43 After allyl alcohol injury, type 0 cells precede the appearanc

44 ond isomerization between a previously known allyl alcohol intermediate and a hindered 2-(2-halopheny

45 Elimination of LiOH from the lithiated allyl alcohol is found to result in the diene product.

46 The hydroxyl hydrogen of allyl alcohol is readily abstracted by either oxygen ada

47 Simple allyl alcohol is shown to be an ideal synthetic equivale

48 lanation for the few special cases where the allyl alcohol is the dominant or exclusive product.

49 donor/acceptor rhodium carbenoids and chiral allyl alcohols is a convergent C-C bond forming process,

50 ch to nonracemic beta,beta-diarylsubstituted allyl alcohols is described.

51 assembly, imparting the ability to catalyze allyl alcohol isomerization.

52 demonstrate that the reaction mechanism for allyl alcohol oxidation is influenced by the relative pr

53 hydroxyl species are shown to be active for allyl alcohol oxidation, but each displays a different p

54 The allyl alcohol product ratios from the vinylalumination o

55 compared to other CAPs, where both diol and allyl alcohol products compete with each other.

56 nly gaseous hydrocarbon product evolved from allyl alcohol reaction on O-covered Mo(110).

57 r selectable or screenable phenotypes (adh1, allyl alcohol resistance; tt4, lack of anthocyanins in t

58 to acetaminophen, carbon tetrachloride, and allyl alcohol, respectively.

59 agenized populations of AOX-induced cells to allyl alcohol selectively kills AOX-containing cells.

60 ective ring-opening reaction of chiral epoxy-allyl alcohols (Sharpless conditions as the key strategi

61 one another, even in the apparently flexible allyl alcohol side chain (-CH horizontal lineCH-CH(2)OH)

62 ted from insertion of palladium to O-H of an allyl alcohol, that is responsible for the C-O bond clea

63 on of PR/S-Ir-pi-allyl intermediate from the allyl alcohol, the diastereocontrol arises due to the di

64 The Rh-catalyst oxidizes allyl alcohol to its carbonyl derivative, and the in sit

65 ovide evidence that the partial oxidation of allyl alcohol to its corresponding aldehyde, acrolein, o

66 uccessfully relayed via proton exchange from allyl alcohol to various target molecules.

67 ntified the system propargyl alcohol + pH(2) allyl alcohol to yield (1)H polarization in excess of P

68 of cationic intermediates generated from CF3-allyl alcohols under reaction conditions.

69 ification reaction between vinyl acetate and allyl alcohol was significantly attenuated (k(vis/UV) =

70 The catalytic hydrogenation of allyl alcohol was significantly enhanced in the presence

71 The obtained allyl alcohols were applied in the synthesis of nonracem

72 The reactions of 2-propen-1-ol (allyl alcohol) were studied on clean and O-covered Mo(11

73 metathesis of various terminal acrylates and allyl alcohols, which enables facile and selective const

74 metathesis of various terminal acrylates and allyl alcohols, which enables facile and selective const

75 ophile in this reaction to generate branched allyl alcohols with good regio- and enantioselectivities

76 The rhodium-catalyzed reaction of racemic allyl alcohols with methyl phenyldiazoacetate or methyl