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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 roceed in part by way of the intermediacy of trimethylene carbonate, which was observed as a minor pr
18 tral poly(ethylene oxide) block and terminal trimethylene carbonate/dithiolane blocks.
19 c carbonates containing pendant dithiolanes (trimethylene carbonate/dithiolane, TMCDT) from poly(ethy
20 in which G* represents guanines linked via a trimethylene chain between N(2) positions.
21           The cross-links are unstable and a trimethylene cross-link has been used as a surrogate for
22                                          The trimethylene cross-link has now been studied in a GpC mo
23            Melting studies indicate that the trimethylene cross-link is thermodynamically less stable
24 e 5'-d(CpG) sequence and is skewed about the trimethylene cross-link.
25 esis of a polyamine-based amino acid, lysine-trimethylene(diNosyl)-spermine(triBoc) with Dde or Fmoc
26 solation from carbon-carbon coupling of 4,4'-trimethylene-dipyridine (tmdp) in the absence of organic
27  to the reactions of papain with a series of trimethylene disulphide reactivity probes.
28 o[a]pyrene-guanine adduct, and an artificial trimethylene insert shows that each of these three lesio
29 AGTCC)-3'.5'-d(GGACTCGCTAGC)-3' (X = N(2)-dG-trimethylene link-KWKK).
30  lysine of the peptide KWKK conjugated via a trimethylene linkage to the N(2)-dG amine positioned in
31 1-tris(diphenylphosphinomethyl)ethane, TMM = trimethylene methane) provides an efficient catalytic sy
32                                              Trimethylene N-oxide (TMAO), a proatherogenic molecule,
33 tem D-br-D*(+) [where br can be an aliphatic trimethylene or an aromatic (poly)phenylene bridge] to b
34 udies on the beta-selective glycosidation of trimethylene oxide (TMO) using mannosyl iodides.
35 of one or more loop riboses to more flexible trimethylene phosphate(s) contributes favorably to the e
36 r lay approximately in a plane such that the trimethylene tether and probably the malondialdehyde tet
37 ludes making an isosteric replacement of the trimethylene tether by malondialdehyde.
38 n imidazoles and 1,2,4-triazines linked by a trimethylene tether from the imidazole N1 position to th
39 h respect to the C(alpha) or C(gamma) of the trimethylene tether, respectively.
40 ethylene tetranitrate (HMX), and cyclo-1,3,5-trimethylene trinitramine (RDX)).

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