ライフサイエンスコーパス: divinyl

1 yl-1,5-disubstituted 1,2,3-triazoles and C/N-divinyl-1,5-disubstituted 1,2,3-triazoles.

2 1,1-Divinyl-2-phenylcyclopropanes are entry points to a rich

3 ed as well as the polytransesterification of divinyl adipate and 1,4-butanediol.

4 conversion of Ox-ynamides into Ox-activated divinyl and aryl vinyl ketones that undergo facile Nazar

5 yl siloxane) (PDMS) over the commercial PDMS/divinyl benzene (DVB) extraction phase.

6 il was combined with a bile salt derivative, divinyl benzene (DVB), and a photo-cross-linker above it

7 temperature-controlled alkalated polystyrene divinyl benzene column.

8 orb cartridge containing 10 g of polystyrene divinyl benzene copolymer beads with a biocompatible pol

9 Michael-type addition to trivinylphosphine, divinyl(benzyl)phosphine, or divinyl(phenyl)phosphine in

10 procedure for the asymmetric epoxidation of divinyl carbinol (3) was described, and the product was

11 ymmetrizing enantioselective diboration of a divinyl carbinol derivative and high-yielding late-stage

12 only 12 types of chlorophylls (Chl a, b, d; divinyl-Chl a and b; and 8(1)-hydroxy-Chl a) and bacteri

13 eous diversification of marine lineages with divinyl chlorophyll b and phycobilisomes as photosynthet

14 It catalyzes the conversion of divinyl chlorophyllide (Chlide) a to monovinyl Chlide a

15 copolymerization of a monovinyl monomer and divinyl cross-linker as well as surfactants with latent

16 rent linear macroinitiator (MI) species by a divinyl cross-linker, such as divinylbenzene.

17 s in water and then were cross-linked by the divinyl cross-linkers.

18 ls-Alder cycloadditions, Cope rearrangement, divinyl cyclopropane-Cope rearrangement, and C-C cleavag

19 Ozonolysis of the 2,6-divinyl derivative of a naphthalene diimide (NDI) afford

20 ysical properties of copolymers derived from divinyl double decker (DD) SQs, [vinyl(Me)Si(O(0.5) )(2)

21 c heterogeneity is rooted mainly in parallel divinyl (DV) and monovinyl (MV) biosynthetic routes inte

22 cid and 9-hydroperoxy linolenic acid yielded divinyl ether fatty acids (colneleic acid and colnelenic

23 e the versatility of this approach, tailored divinyl ether monomers were polymerized with triethylene

24 ional groups can be designed into either the divinyl ether or dithiol monomer.

25 erminant of the tissue specific synthesis of divinyl ether oxylipins.

26 he first identification of a cDNA encoding a divinyl ether synthase and establishment of the enzyme a

27 ndicate that developmental expression of the divinyl ether synthase gene is an important determinant

28 analysis revealed the existence of a single divinyl ether synthase gene located on chromosome one of

29 ings, root tissue was the major site of both divinyl ether synthase mRNA accumulation and enzyme acti

30 itol was polymerized with triethylene glycol divinyl ether to yield a polymer with pendant diols and

31 Monosilylated divinyl ethers can be isomerized using a cationic iridiu

32 adily available activated alkynes delivering divinyl ethers is reported.

33 )=CHCH(2)CH(OR)(2) acetals, and they cyclize divinyl ethers to analogous cyclic acetals.

34 a [3,3]sigmatropic rearrangement of the N,O-divinyl hydroxylamines to corresponding imino-aldehydes

35 In one case, a divinyl ketone (ketone 6) undergoes Nazarov cyclization

36 The Nazarov cyclizations of a divinyl ketone catalyzed by a BINOL phosphoric acid or H

37 teraction of a nonconjugated alkene with the divinyl ketone pi system in the endo transition state an

38 ntributions of different substituents on the divinyl ketone.

39 entailing the Nazarov electrocyclization of divinyl ketones and nucleophilic addition of the resulti

40 azarov cyclization precursors, alpha-carboxy divinyl ketones C.

41 econd effect in the ring closures of several divinyl ketones explains the reduced selectivity of thes

42 ations, to afford spirocyclic compounds from divinyl ketones in the presence of 1 equiv of copper(II)

43 A variety of different divinyl ketones including aromatic systems undergo the i

44 Silver-catalyzed silylene transfer to divinyl ketones provided 2-silyloxy-1,3-dienes with cont

45 ization of simple, acylic, alkyl-substituted divinyl ketones using our recently disclosed strong and

46 As reaction products, 2,4-diene-6-ols or divinyl ketones were obtained.

47 ov/Wagner-Meerwein rearrangement sequence of divinyl ketones.

48 methylene pronucleophiles to nonsymmetrical divinyl ketones.

49 ned with the commercial availability of many divinyl monomers and the robustness of free radical poly

50 ers by direct free radical polymerization of divinyl monomers controlled by a cobalt chain transfer c

51 eospecificity in the polymerization of polar divinyl monomers including vinyl methacrylate (VMA), all

52 specific, and living polymerization of polar divinyl monomers, enabled by chiral ansa-zirconocenium c

53 polymerization of three representative polar divinyl monomers, including vinyl methacrylate (VMA), al

54 perfectly chemoselective for all four polar divinyl monomers, proceeding exclusively through conjuga

55 the oligomerization of butadiene to generate divinyl(oligocyclobutane), a microstructure of poly(buta

56 nrealized telechelic microstructure of (1,n'-divinyl)oligocyclobutane.

57 the retro-[2 + 2] depolymerization of (1,n'-divinyl)-oligocyclobutane to butadiene dimers.

58 hiol-ene strategy, where the multithiols and divinyl oligomers were designed to contain only C, H, an

59 which accumulated both monovinyl-PChlide and divinyl-PChlide and excreted PChlides into the medium.

60 vinylphosphine, divinyl(benzyl)phosphine, or divinyl(phenyl)phosphine in [(eta(5)-Cp(R))Fe(diphosphin

61 yndiospecific coordination polymerization of divinyl polar monomers developed through this work, has

62 X (Proto IX), Mg-proto, Mg-proto MME and 3,8-divinyl protochlorophyllide a (DV-Pchlide) levels, but t

63 atmospheric O2 levels, AcsFI synthesizes 3,8-divinyl protochlorophyllide from Mg-protoporphyrin IX mo

64 he mutant cells secrete large amounts of 3,8-divinyl-protochlorophyllide a into the growth medium and

65 nant BciA reduces the C-8 vinyl group of 3,8-divinyl-protochlorophyllide in vitro.

66 ate that CT1063, renamed bciA, encodes a C-8 divinyl reductase in C. tepidum.

67 -type addition between biaryl phosphines and divinyl silanes, this strategy enables the efficient pre

68 A multifunctional cross-linking initiator, divinyl sulfone (DVS), is firstly pre-embedded into pero

69 d carbon nanotubes and silica supports using divinyl sulfone and genipin crosslinkers.

70 Divinyl sulfone crosslinked HA hydrogels were converted

71 GkASNase immobilized on silica support via divinyl sulfone exhibited a 28.9-fold enhancement in the

72 Divinyl sulfone reacts at pH 8-9 with the alpha-amino gr

73 Trifluoromethyl-substituted divinyl sulfones prepared by this protocol can be readil

74 he surface of the water with water-insoluble divinyl sulfones upon microwave irradiation at 150 degre