ライフサイエンスコーパス: trimethylene

1 ducts between the high explosive cyclo-1,3,5-trimethylene-2,4,6-trinitramine (RDX) and halide anions

2 hree common military explosives: cyclo-1,3,5-trimethylene-2,4,6-trinitramine (RDX), nitroglycerin (NG

3 ly used secondary explosive RDX (cyclo-1,3,5-trimethylene-2,4,6-trinitramine).

4 The trimethylene- and biphenylene-bridged cations D(CH(2))(3

5 inomethyl]-1-methylpyridinium chloride, 1,1'-trimethylene bis-(4-hydroxyimino methyl)-pyridinium dibr

6 16-tetraaza[5,5]paracyclophane (Me3C), a bis-trimethylene bridged bis-p-phenylene diamine (PD), and i

7 The trimethylene-bridged amine/borane frustrated Lewis pair

8 report synthesis and investigation of doubly trimethylene-bridged tetrabenzyl-p-phenylenediamine 1(Bz

9 possible, but Me3C2+ has doubly gg N(CH2)3N trimethylene bridges and both N,N and C,C distances betw

10 ioabsorbable, macroporous, polyglycolic acid-trimethylene carbonate (PGA-TMC) membrane combined with

11 w bioabsorbable, synthetic polyglycolic acid/trimethylene carbonate (PGA/TMC) barrier membrane with a

12 nitiating the ring-opening polymerization of trimethylene carbonate (TMC) from methyl cholate through

13 mol (-1) for ring-opening polymerization of trimethylene carbonate and 107.6 kJ x mol (-1) for copol

14 cluding commercially available l-lactide and trimethylene carbonate produced novel copolymers.

15 Polymerization of trimethylene carbonate was also performed with the reduc

16 s polymerization of epsilon-caprolactone and trimethylene carbonate was investigated.

17 ene glycol)-block-poly(caprolactone-gradient-trimethylene carbonate) (PEG-P(CLgTMC)), with tetrapheny

18 obic segment of a poly(ethylene glycol)-poly(trimethylene carbonate) block copolymer, of which the ca

19 ng a terpolymer comprising poly p-dioxanone, trimethylene carbonate, and glycolide.

20 roceed in part by way of the intermediacy of trimethylene carbonate, which was observed as a minor pr

21 tral poly(ethylene oxide) block and terminal trimethylene carbonate/dithiolane blocks.

22 c carbonates containing pendant dithiolanes (trimethylene carbonate/dithiolane, TMCDT) from poly(ethy

23 in which G* represents guanines linked via a trimethylene chain between N(2) positions.

24 The cross-links are unstable and a trimethylene cross-link has been used as a surrogate for

25 The trimethylene cross-link has now been studied in a GpC mo

26 Melting studies indicate that the trimethylene cross-link is thermodynamically less stable

27 e 5'-d(CpG) sequence and is skewed about the trimethylene cross-link.

28 esis of a polyamine-based amino acid, lysine-trimethylene(diNosyl)-spermine(triBoc) with Dde or Fmoc

29 solation from carbon-carbon coupling of 4,4'-trimethylene-dipyridine (tmdp) in the absence of organic

30 to the reactions of papain with a series of trimethylene disulphide reactivity probes.

31 o[a]pyrene-guanine adduct, and an artificial trimethylene insert shows that each of these three lesio

32 AGTCC)-3'.5'-d(GGACTCGCTAGC)-3' (X = N(2)-dG-trimethylene link-KWKK).

33 lysine of the peptide KWKK conjugated via a trimethylene linkage to the N(2)-dG amine positioned in

34 tion of a bifunctional allylating reagent, a trimethylene methane dianion equivalent, that provides a

35 1-tris(diphenylphosphinomethyl)ethane, TMM = trimethylene methane) provides an efficient catalytic sy

36 Trimethylene N-oxide (TMAO), a proatherogenic molecule,

37 tem D-br-D*(+) [where br can be an aliphatic trimethylene or an aromatic (poly)phenylene bridge] to b

38 udies on the beta-selective glycosidation of trimethylene oxide (TMO) using mannosyl iodides.

39 of one or more loop riboses to more flexible trimethylene phosphate(s) contributes favorably to the e

40 lly biobased engineering thermoplastic, poly(trimethylene terephthalate) (PTT), was combined with 20

41 r lay approximately in a plane such that the trimethylene tether and probably the malondialdehyde tet

42 ludes making an isosteric replacement of the trimethylene tether by malondialdehyde.

43 n imidazoles and 1,2,4-triazines linked by a trimethylene tether from the imidazole N1 position to th

44 ecular analogues (isoquinolinium linked by a trimethylene tether to alkyl benzenes) that proved to be

45 h respect to the C(alpha) or C(gamma) of the trimethylene tether, respectively.

46 ethylene tetranitrate (HMX), and cyclo-1,3,5-trimethylene trinitramine (RDX)).