ライフサイエンスコーパス: allylamine

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

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

2 e modified by pulsed rf plasma deposition of allylamine.

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

4 ates are precursors to enantioenriched epoxy allylamines.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。