ライフサイエンスコーパス: divinyl

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

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

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

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

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

6 temperature-controlled alkalated polystyrene divinyl benzene column.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

28 Monosilylated divinyl ethers can be isomerized using a cationic iridiu

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

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

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

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

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

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

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

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

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

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

39 methylene pronucleophiles to nonsymmetrical divinyl ketones.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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