ライフサイエンスコーパス: allyl alcohol

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

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

3 ping of the quinonemethide intermediate with allyl alcohol.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 The allyl alcohol product ratios from the vinylalumination o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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