ライフサイエンスコーパス: butylamine

1 his product showed the incorporation of tert-butylamine.

2 -alkylamines, such as N,N-diethyl-2-methyl-2-butylamine (1, t-PentNEt2), N,N-diethyl-2,3-dimethyl-2-b

3 erved in the reduction of N-benzilidene-tert-butylamine (11) at -48 degrees C (k(OH)/k(OD) = 0.89 +/-

4 (1, t-PentNEt2), N,N-diethyl-2,3-dimethyl-2-butylamine (2, t-HexNEt2), N,N-diethyl-2,3,3-trimethyl-2

5 2, t-HexNEt2), N,N-diethyl-2,3,3-trimethyl-2-butylamine (3, t-HeptNEt2), and N,N-diethyl-1,1,3,3-tetr

6 ion of a 1,6-adduct between an o-quinone and butylamine (3-n-butylamino-5-ethyl-1,2-benzoquinone, 13)

7 f o-alkynyl aldehyde 4a-t and 5a-p with tert-butylamine 6 under mild reaction conditions is described

8 thylamine, ethylenediamine, hydroxylamine, n-butylamine, adenosine, cytosine, guanine, thymine, and l

9 With butylamine and a large concentration (0.5 M) of added Na

10 of 2-bromo-2-nitro-1,3-propanediol with tert-butylamine and formaldehyde to yield 1,3-di-tert-butyl-5

11 For t-butylamine and methylamine, the amount of labeling incre

12 oncerning these labeling reactions, t-[(14)C]butylamine and phenylhydrazine were employed as probes.

13 ng methylamine, ethylamine, n-propylamine, n-butylamine, and 1,5-diamino pentane as mimics for the si

14 tes (72, 190, and 162 s(-1) for methylamine, butylamine, and benzylamine, respectively).

15 pectively, for the reactions of methylamine, butylamine, and benzylamine.

16 ated symmetric dimer in DMEA, N,N-dimethyl-n-butylamine, and N-methylpyrrolidine.

17 n-related odorants, such as isovaleric acid, butylamine, and several ketones and oxocarboxylic acids.

18 ty and thus showed a higher selectivity to n-butylamine as compared to nanopolyhedra.

19 rtho borylation could be achieved using tert-butylamine as the traceless protecting/directing group,

20 and shape controls, this work develops a new butylamine-based surface treatment approach for removing

21 With optimized film compositions, 1-butylamine can be detected in the gas phase to levels ap

22 Cleavage and deprotection with aqueous tert-butylamine cocktail gave 5-Tamra-functionalized DNA as w

23 cted by a weaker reducing agent, borane-tert-butylamine complex.

24 varying basicities and nucleophilicities: n-butylamine, diethylamine, triethylamine, N-methylpyrroli

25 via a catalytic CBS asymmetric reduction, t-butylamine displacement of the chlorohydrin, and a conju

26 hypusine synthase, employing spermidine as a butylamine donor.

27 quent in situ ammonium/amine substitution by butylamine enables quantum dots to be capped by butylamm

28 nked, photoactivable 4-p-(azidosalicylamido)-butylamine group.

29 n reactions, with a selectivity pattern of 1-butylamine > 1-propylamine > pyridine > triethylamine >

30 hylamine > methylamine > diethylamine > tert-butylamine > ammonia.

31 urements and simulations, examining the tert-butylamine + H2 + H2O hydrate system, now suggest that H

32 imulation with a live bacterial product, iso-butylamine (IBA), but not to dead bacteria or LPS.

33 N-acetyl-dl-homocysteine thiolactone with n-butylamine in THF and CHCl3.

34 These quantum dots have benzoate (X) and n-butylamine (L) ligands and tetrahedral (Td) shape with e

35 ions, it is found that C3 propylamine and C4 butylamine linkers exhibit the highest probability of re

36 A mixture (1:1:2) of t-butylamine:methanol:water is used for cleavage and depro

37 cing agent suggests an intermediate with the butylamine moiety derived from spermidine attached throu

38 iments showing efficient transfer of labeled butylamine moiety from enzyme intermediate to eIF-5A pre

39 ation of deoxyhypusine by conjugation of the butylamine moiety of spermidine to the epsilon-amino gro

40 on with primary and secondary amines such as butylamine, morpholine, and aniline derivatives.

41 S, Se; and L = ethylamine, n-propylamine, n-butylamine, n-amylamine, n-hexylamine).

42 ethyldecanoic acid amide, 4 (6 Li/mol), in t-butylamine/N, N'-dimethylethylenediamine gave N-methylde

43 sodi-n-propylamine (NDPA), and N-nitrosodi-n-butylamine (NDBA) and their precursors.

44 matic increase of substitution rates by tert-butylamine on alpha-bromopropiophenones is observed with

45 upon treatment of PSII with either t-[(14)C]butylamine or [(14)C]phenylhydrazine.

46 r threo- and erythro-N,N-dimethyl-3-phenyl-2-butylamine oxide have been investigated using QM/MM calc

47 Replacing the n-butylamine Schiff base normally chosen to mimic the satu

48 nts such as borane-ammonia (AB), borane-tert-butylamine (TBAB), and sodium tetrahydridoborate (THB) i

49 PbSe, PbS) by various Lewis bases (L = tri-n-butylamine, tetrahydrofuran, tetradecanol, N,N-dimethyl-

50 aved products confirmed the addition of tert-butylamine to the minor product.

51 etrahydrofuran, tetradecanol, N,N-dimethyl-n-butylamine, tri-n-butylphosphine, N,N,N',N'-tetramethylb

52 ine and alpha-cyano-4-hydroxycinnamic acid + butylamine) were investigated, and possible mechanisms a

53 an be selectively cleaved with methanol/tert-butylamine, while the ester group at the sn-1-position r