ライフサイエンスコーパス: primary amide

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

2 re in aqueous base to give the corresponding primary amide.

3 y the reaction of 2-aminobenzyl alcohol with primary amides.

4 oinduced, copper-catalyzed monoalkylation of primary amides.

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

6 odimeric complexes with carboxylic acids and primary amides.

7 (OR)](+), in the presence of polyhalogenated primary amides.

8 from amines and carboxylic acids, esters, or primary amides.

9 previous direct method, which was limited to primary amides.

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

11 trogen atom transfer offers facile access to primary amides after deprotection.

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

13 0-308 nm light to cleanly release N-terminal primary amide and C-terminal indolylenamide fragments.

14 Of particular concern is that 21 primary amide and fatty acid surfactants were introduced

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

16 s imperative in interpreting data concerning primary amides and fatty acids when employing plastic la

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

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

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

20 ighlight the substituent on the indole and a primary amide as groups driving selectivity.

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

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

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

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

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

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

27 Primary amide-directed ortho-olefination of benzamide us

28 process is applicable to the N-alkylation of primary amides employing unactivated alkyl iodides and b

29 MCTs artificially introduced 10 additional primary amides extraneous to serum samples.

30 y results indicate high regioselectivity for primary amide formation in the diol-Ritter sequence.

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

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

33 ction using a simple and weakly coordinating primary amide group in the presence of an inexpensive Ru

34 This is the first report where native primary amide has been utilized as a weakly coordinating

35 bromoesterification reaction is inhibited by primary amides, imides, hydantoins, and secondary cyclic

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

37 d calcium nitride afforded the corresponding primary amides in a transformation that was compatible w

38 zation of aldehydes with NH(2)OR to valuable primary amides in nonconventional aqueous media with exc

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

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

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

42 -9-octadecenamide), an endogenous fatty acid primary amide, is a predominant component of meibum when

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

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

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

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

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

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

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

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

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

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

53 rd, metal-catalyzed silylative conversion of primary amides to nitriles is emerging as a promising ap

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

55 n exhibits chemo-selectivity, where only the primary amide undergoes C-H annulation, leaving the seco

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

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

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

59 A selective ortho-olefination of primary amides yields valuable motifs for pharmaceutical