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1       They represent a new type of binuclear boron compound.
2 s downstream functionalizations of the alkyl boron compounds.
3 ntial applications of the stimuli-responsive boron compounds.
4 ctive coupling of dinitrogen with low-valent boron compounds.
5 al position enables the self-assembly of the boron compound 2d to form a fluorescent vesicle, which i
6                                Additionally, boron compound 2d was found to serve as a dye for cell i
7                                          The boron compounds 3 and 4 have shown low cytotoxicity acti
8                                  These allyl boron compounds act as allylation reagents with aldehyde
9 s were validated by analyzing stoichiometric boron compounds and applied to samples such as boron car
10 ical shifts of the hypercoordinated hydriodo boron compounds and the 13C NMR chemical shifts of the c
11  a cross-coupling after transmetalation with boron compounds and to a homocoupling after transmetalat
12                                  Novel allyl boron compounds are readily synthesized via rearrangemen
13 e with terminal N-substituted (SPD-1, SPM-1) boron compounds, are greater than those of SPD/SPM.
14                          The new N,C-chelate boron compounds B(2-phenylazolyl)Mes2 [Mes = mesityl; az
15 mbers of very rare classes of functionalized boron compounds (boron azide, nitro compound, nitrous es
16 onstrate how the interactions of sugars with boron compounds can be combined with transition metal ca
17 imesitylboron compounds, the new C,C-chelate boron compounds have a much larger HOMO-LUMO energy gap
18                                              Boron compounds have a rich history in energy storage ap
19                                      Layered boron compounds have attracted significant interest in a
20                                              Boron compounds have been traditionally regarded as "Lew
21                        Recently, a number of boron compounds having a rhomboidal B(4) framework have
22  treatment, BA emerges again as an efficient boron compound in the case of selected tumour types.
23                  An electron-rich monovalent boron compound is used as a Lewis base to prepare adduct
24 n interesting feature of elemental boron and boron compounds is the occurrence of highly symmetric ic
25 trol chemoselective functionalization of bis(boron) compounds is by engendering different Lewis acidi
26 ture Database counts 1253 entries for binary boron compounds!), it is surprising that the application
27             A commercially available allenyl-boron compound or a monosubstituted allene may be used.
28 have been confined to the formation of alkyl boron compounds via C(sp(3)) insertion into a C-B bond.
29 ration to furnish the differentiable 1,2-bis(boron) compounds with high levels of regio- and enantioc