ライフサイエンスコーパス: primary amide

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1 he unique hydrogen-bonding properties of the primary amide.

2 oinduced, copper-catalyzed monoalkylation of primary amides.

3 lpha,alpha-branched primary alkylamines, and primary amides.

4 odimeric complexes with carboxylic acids and primary amides.

5 oy N,N-dialkylformamide dimethyl acetals for primary amide activation, producing N'-acyl-N,N-dialkylf

6 cludes alpha-iodo ketones, esters, nitriles, primary amides, alpha-fluorinated halo-acetates and perf

7 0-308 nm light to cleanly release N-terminal primary amide and C-terminal indolylenamide fragments.

8 A variety of different primary amides and amines are found to undergo efficient

9 igh-yielding, one-step borane reduction of a primary amide, and a stereoselective substitution of the

10 ydrogen-bonding functions--carboxylic acids, primary amides, and boronic acids--within a multicompone

11 novel N-methyl-containing amines and amides, primary amides, and novel N-acetylated sugars, which tog

12 iimide reagent and is assumed to result in a primary amide bond between the polymer film and the modi

13 Secondary or tertiary amides may replace the primary amide but follow a well defined relationship req

14 These substitutions include the C2 primary amide, C4 dimethylamine, and the C12a tertiary a

15 Secondary and primary amides can be masked as N-Ns amides to undergo r

16 on how a nominally nonnucleophilic group, a primary amide, can become activated in a protein active

17 ratures, enabling the selective reduction of primary amides, carbonates, and ureas in high yields.

18 placing an amine group (K side chain) with a primary amide group (Q side chain) weakens the hydrophob

19 tion leading to the selective formation of a primary amide group from a chemically inert alkyl group.

20 poration of water solubilizing groups to the primary amide in 2 without protecting group manipulation

21 two nonionic polar groups (primary amine and primary amide) influence hydrophobic interactions of nei

22 Herein a simple primary amide is described that achieves the selective s

23 ver-cocatalyzed conversion of aldoximes into primary amides is reported.

24 -9-octadecenamide), an endogenous fatty acid primary amide, is a predominant component of meibum when

25 iple bond W) = 2.337(2) A), which is a rare, primary amide M2X4Y2 species.

26 Of the naturally occurring fatty acids, the primary amide of oleic acid (oleamide) is the most effec

27 ounds, which are the first stable homoleptic primary amides of iron(II), were obtained by the transam

28 hibitors fall into two classes of fatty acid primary amides of which oleamide and arachidonamide are

29 anine at the C-terminus was converted to the primary amide or to an extended structure containing a t

30 en made with regard to the transamidation of primary amide substrates, secondary amide transamidation

31 It is applicable to the functionalization of primary amides, sulfonamides, and other N-functional gro

32 Despite their lack of a primary amide terminals allowing the formation of the hy

33 Oleamide is an endogenous fatty acid primary amide that possesses sleep-inducing properties i

34 Oleamide is an endogenous fatty acid primary amide that possesses sleep-inducing properties i

35 nitrogen nucleophiles such as carbazoles and primary amides undergo C-N coupling with alkyl halides u

36 aleramide to determine the dependence of the primary amide vibrations on amide HB.

37 The C-terminal primary amide was replaced with a benzimidazole ring, wh

38 Two protocols for the transamidation of primary amides with primary and secondary amines, formin

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