ライフサイエンスコーパス: allylamine

1 poly[vinylpyridine Os(bisbipyridine)2Cl]-co-allylamine.

2 e modified by pulsed rf plasma deposition of allylamine.

3 of the thermodynamically stable C-N bond of allylamine.

4 he transformation (S,E)-isomers leads to (R)-allylamines.

5 to provide a broad range of N-functionalized allylamines.

6 ates are precursors to enantioenriched epoxy allylamines.

7 )allylamide 1 and N-lithio-N-(trimethylsilyl)allylamine 2 compounds.

8 culations also suggest that deprotonation of allylamine 2 exclusively at the cis-vinylic position is

9 liphatic, cyclic/acyclic, secondary/tertiary allylamines (70 examples), including drugs or their deri

10 static-induced aggregation of ConA with poly(allylamine), a positively charged polymer, by shielding

11 ere modified by plasma polymerization, using allylamine, acrylic acid and 2-methyl-2-oxazoline as pre

12 ithium anion of N-allyl imine (prepared from allylamine and benzophenone) to alpha,beta-unsaturated e

13 oduced by pulsed rf plasma polymerization of allylamine and deposited directly on a MALDI probe, can

14 reby, easily accessible Boc-protected N-aryl-allylamine and homoallylamine derivatives were reacted w

15 MIP-Gly NPs synthesized using allylamine and squaramide-based monomers appeared most s

16 allenes with high stereoselectivity to the Z-allylamines and allow the hydroamination of a trisubstit

17 A variety of functionalized N-allylamines and N-allylsulfonamides are synthesized by P

18 ace of the transistors is modified with poly(allylamine), and the effect of phosphate binding on the

19 tilizes very common chemicals, benzaldehyde, allylamine, and cinnamic acid, via intramolectular [2+2]

20 silole is functionalized by hydrosilation of allylamine, and the colloid is prepared by the rapid add

21 ))-H activation and Z-selective arylation of allylamines are reported.

22 pyridil redox relay sites on polycation poly(allylamine) backbone efficiently work as a molecular "wi

23 N-(Trialkylsilyl)allylamines can be deprotonated at the cis-vinylic posit

24 N-Lithio-N-(trialkylsilyl)allylamines can be deprotonated in the presence of ether

25 een the flavin cofactor N(5) with the distal allylamine carbon atom as well as the absence of the flu

26 has emerged as a powerful tool to construct allylamines, common motifs in molecular therapeutics.

27 The Pd(II)-catalyzed arylation of an allylamine containing both gamma-C(sp(2))-H and gamma-C(

28 of a formal (4+2) cycloaddition between the allylamine derivatives and allenes and is initiated by a

29 ied nucleotides were synthesized by coupling allylamine-dUTP to the succinimidyl-ester derivatives of

30 nse to several clinical antifungals (azoles, allylamines, echinocandins) that target the ER or cell w

31 lic amination that can directly afford alkyl allylamines, enabled by the reactivity of thianthrene-ba

32 -naphthalenetetracarboxylic dianhydride with allylamine, followed by LiAlH(4) reduction and subsequen

33 the highly enantioselective isomerization of allylamines, followed by enamine exchange, and subsequen

34 able using aminopropyl trimethoxy silane and allylamine for post-polymerization modification, respect

35 Although Heck-type gamma-arylations of allylamines have generally afforded the E-cinnamylamines

36 NPs) functionalized with the polycation poly(allylamine HCl) in a manner that depends on the NOM-to-D

37 rochloride (PAH) and its monomeric precursor allylamine hydrochloride (AH) with lipid bilayers.

38 tical fiber by immersion alternately in poly-allylamine hydrochloride and in poly-1-[p-(3'-carboxy-4'

39 polyelectrolyte multilayers comprising poly(allylamine hydrochloride) (PAH) and poly(sodium 4-styren

40 ssembled onto the LPG with the aid of a poly(allylamine hydrochloride) (PAH) polycation layer.

41 ene oxide (GO) sheets and the TiO2 NFs, poly(allylamine hydrochloride) (PAH) was used to induce a pos

42 d with a cationic weak polyelectrolyte (poly(allylamine hydrochloride) (PAH)) for the label-free elec

43 ticles (AuNPs) were wrapped with 15 kDa poly(allylamine hydrochloride) (PAH), and three purification

44 phite oxide in the presence of cationic poly(allylamine hydrochloride) (PAH).

45 odified poly(acrylic acid) (PAA-BP) and poly(allylamine hydrochloride) (PAH-BP).

46 -by-layer self-assembly of a flocculant poly(allylamine hydrochloride) and its tautomer poly(acrylic

47 the channels with alternating layers of poly(allylamine hydrochloride) and poly(styrene sulfonate).

48 lt up with layer-by-layer deposition of poly(allylamine hydrochloride) and sodium silicate, followed

49 he conditions tested, a single layer of poly(allylamine hydrochloride) completely stops chitosan diff

50 ltilayer film of poly(acrylic acid) and poly(allylamine hydrochloride) followed by replicate producti

51 enylene ethynylene) backbone, aPPE, and poly(allylamine hydrochloride) PAH polycation.

52 er 188 and 0.1% of the cationic polymer poly(allylamine hydrochloride) showed an average nanoparticle

53 te capping agents in the supernatant of poly(allylamine hydrochloride)-coated nanoparticles significa

54 In particular, exposure to the poly(allylamine hydrochloride)-coated particles reduces the a

55 n of sequence-specific nucleic acids on poly(allylamine hydrochloride)-functionalized CaCO3 core micr

56 itrate and the cationic polyelectrolyte poly(allylamine hydrochloride).

57 x 10(5) with a 500 nM concentration of poly(allylamine hydrochloride).

58 id) side chains with a cationic linear poly (allylamine hydrochloride).

59 ng apolyelectrolyte multilayer (PEM) of poly(allylamine hydrochloride)/poly(sodium 4-styrenesulfonate

60 ulations to quantify the interaction of poly(allylamine) hydrochloride (PAH) and its monomeric precur

61 nation nanodiamond covalently linked to poly(allylamine) hydrochloride as a model system, we demonstr

62 e of 3,N-dilithio-N-(tert-butyldimethylsilyl)allylamine identified three major aggregates in THF (mon

63 cture of N-lithio-N-(tert-butyldimethylsilyl)allylamine in the presence of nBuLi identified amide/nBu

64 reaction of 1,3-cyclodiketone, furfural, and allylamine in toluene.

65 ed chemical vapor deposition (iCVD) and poly(allylamine) (PAAm) via a plasma polymerization process,

66 lammonium chloride (PDAC) outperforming poly(allylamine), poly(lysine), and poly(arginine) in polycat

67 e ring present in the GMA upon reaction with allylamine produces the vinylated MWCNT (MWCNT-CH = CH2)

68 s immobilized by a cobaltocene-modified poly(allylamine) redox polymer on the electrode surface (DH/C

69 steps: (i) allylic oxidation of the starting allylamine to corresponding unsaturated allylamide with

70 mercuri-UDP-HexNAc and then attachment of an allylamine to the 5 position to give 5-(3-amino)allyl-UD

71 ed oxidation of this type of cyclic tertiary allylamine to the corresponding dihydropyridinium metabo

72 in three steps: (1) aza-Michael addition of allylamine to tricarbonyl(tropone)iron; (2) Boc-protecti

73 have led to the selective gamma-arylation of allylamines to construct various cinnamylamines with mod

74 carbofunctionalization of highly substituted allylamines to give highly Z-selective trisubsubstituted

75 by reacting the initial catalysts with poly(allylamine) to create an outer layer that is more hydrop

76 Ac photoaffinity probe azido-125I-salicylate-allylamine-UDP-GlcNAc or a similar UDP-GalNAc photoaffin

77 ition to yield 3,N-dilithio-N-(trialkylsilyl)allylamines under mild conditions.

78 ition to yield 3,N-dilithio-N-(trialkylsilyl)allylamines under mild conditions.

79 catalyzed enantioselective hydroamination of allylamines using a chiral BIPHEP-type ligand is reporte

80 for preparing 2,3-epoxyamides from tertiary allylamines via a tandem C-H oxidation/double bond epoxi

81 n the synthesis of nonracemic alpha-tertiary allylamines via stereocontrolled cyanate-to-isocyanate s

82 -beginning from tricarbonyl(tropone)iron and allylamine was accomplished in three steps: (1) aza-Mich

83 ylene glycol, aminopropyl trimethoxy silane, allylamine) was investigated.

84 ng group picolinamide-directed arylations of allylamines were found to be Z-selective.

85 (S,Z)-allyl carbamates provides (S)-teriary allylamines, whereas the transformation (S,E)-isomers le

86 selectively delivers anti-cyclopropanes for allylamines with a removable isoquinoline-1-carboxamide

87 N-(Trialkylsilyl)allylamines with terminal alkyl substituents were report

88 allow the generation of stable dianions from allylamines with terminal alkyl substituents.