ライフサイエンスコーパス: isoamyl

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1 by covalent binding for use in synthesis of isoamyl acetate (IAAc), which has a typical banana flavo

2 etate 39.48 ng mL(-1) (RSD mean value 4.2%), isoamyl acetate 3.88 ng mL(-1) (RSD mean value 3.4%), et

3 Lilial similarly antagonized the response to isoamyl acetate in other ORNs, indicating the effect gen

4 n, the onset and recovery kinetics following isoamyl acetate stimulation are prolonged in the null mi

5 odorants were ethyl acetate, ethyl butyrate, isoamyl acetate, and isoamyl butyrate.

6 acid on sensory perception and volatility of isoamyl acetate, ethyl isobutyrate, ethyl butyrate and e

7 of straight-chain fatty acids, ethyl, hexyl, isoamyl acetates and superior alcohols than the control

8 e AWC-sensed odorants benzaldehyde (Bnz) and isoamyl alcohol (IsoA) and can reciprocally cross-adapt.

9 the analogous alkane of the potent inhibitor isoamyl alcohol (isopentanol), did not.

10 We found that several alcohols, notably isoamyl alcohol and 1-butanol, stimulate filamentous gro

11 lcohol, (Z)-3-hexen-1-ol, coniferyl alcohol, isoamyl alcohol and linolenic acid.

12 The aqueous phase contains some 0.15 M isoamyl alcohol and the unreacted hydrogen peroxide, but

13 nitrite are processed for removal of IPA and isoamyl alcohol by solvent extraction.

14 thidium bromide can be readily removed using isoamyl alcohol extractions combined with intercalator-s

15 itrite remains in the aqueous phase, whereas isoamyl alcohol forms a new organic phase along with the

16 Removal of isoamyl alcohol or traces of isoamyl nitrite is accompli

17 benzyl alcohol; in Corvina, benzyl alcohol, isoamyl alcohol, 1-hexanol, p-cymen-8-ol, 2,3 pinanediol

18 ain of these alcohols, including butanol and isoamyl alcohol, bring about a rapid inhibition of trans

19 t relevant wine higher alcohols (isobutanol, isoamyl alcohol, methionol and beta-phenylethanol) on re

20 he sensory importance of the pair isobutanol-isoamyl alcohol.

21 l hexanoate, ethyl octanoate, butyrolactone, isoamyl alcohols, acetaldehyde, ethyl acetate, 2,3-butan

22 Within the free volatile compounds, isoamyl alcohols, benzaldehyde and guaiacol registered t

23 ile within the bound volatile compounds were isoamyl alcohols, ethyl vanillate and benzoic acid.

24 cetate, ethyl butyrate, isoamyl acetate, and isoamyl butyrate.

25 e glomerular layer responded specifically to isoamyl esters, and other regions preferred ethyl esters

26 isobutyl ketone (DIBK, yield 66%) and methyl isoamyl ketone (MIAK, yield 81%).

27 nd 1,4-oxathiane: tert-butyl methyl sulfide, isoamyl methyl sulfide, ethyl isoamyl sulfide, tert-buty

28 /TFAA (with [emim][CF3COO], [emim][NO3]) and isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH (with [em

29 ty of nitrating systems, namely NH4NO3/TFAA, isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH, Cu(NO3)/

30 , [emim][NO3]) and isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH (with [emim][OTf]) provided the bes

31 amely NH4NO3/TFAA, isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH, Cu(NO3)/TFAA, and AgNO3/Tf2O.

32 ydroperoxide anion (in the aqueous phase) on isoamyl nitrite (in the organic phase).

33 aryl-diazonium chemistry in the presence of isoamyl nitrite followed by condensation reaction of the

34 Removal of isoamyl alcohol or traces of isoamyl nitrite is accomplished by washing the aqueous p

35 and the unreacted hydrogen peroxide, but no isoamyl nitrite.

36 a new organic phase along with the unreacted isoamyl nitrite.

37 lves nitrosation of H2O2 at pH> or = 12.5 by isoamyl or butyl nitrite in mixed solvents of isopropyl

38 Isoamyl- or cyclopropylmethylene-substituted dipyrrole d

39 l sulfide, ethyl isoamyl sulfide, tert-butyl isoamyl sulfide, diisoamyl sulfide, tetrahydrothiophene,

40 ethyl sulfide, isoamyl methyl sulfide, ethyl isoamyl sulfide, tert-butyl isoamyl sulfide, diisoamyl s

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