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1       They represent a new type of binuclear boron compound.
2 al position enables the self-assembly of the boron compound 2d to form a fluorescent vesicle, which i
3                                Additionally, boron compound 2d was found to serve as a dye for cell i
4                                          The boron compounds 3 and 4 have shown low cytotoxicity acti
5                                  These allyl boron compounds act as allylation reagents with aldehyde
6 s were validated by analyzing stoichiometric boron compounds and applied to samples such as boron car
7 ical shifts of the hypercoordinated hydriodo boron compounds and the 13C NMR chemical shifts of the c
8  a cross-coupling after transmetalation with boron compounds and to a homocoupling after transmetalat
9                                  Novel allyl boron compounds are readily synthesized via rearrangemen
10 e with terminal N-substituted (SPD-1, SPM-1) boron compounds, are greater than those of SPD/SPM.
11                          The new N,C-chelate boron compounds B(2-phenylazolyl)Mes2 [Mes = mesityl; az
12 mbers of very rare classes of functionalized boron compounds (boron azide, nitro compound, nitrous es
13 onstrate how the interactions of sugars with boron compounds can be combined with transition metal ca
14 imesitylboron compounds, the new C,C-chelate boron compounds have a much larger HOMO-LUMO energy gap
15                                              Boron compounds have been traditionally regarded as "Lew
16                        Recently, a number of boron compounds having a rhomboidal B(4) framework have
17                  An electron-rich monovalent boron compound is used as a Lewis base to prepare adduct
18 n interesting feature of elemental boron and boron compounds is the occurrence of highly symmetric ic
19 ture Database counts 1253 entries for binary boron compounds!), it is surprising that the application
20             A commercially available allenyl-boron compound or a monosubstituted allene may be used.

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