57312-00-2Relevant articles and documents
Influence of Extended Conjugation on Photophysical/Electronic Properties and Photoelimination of BN-Heterocycles
Shi, Yong-Gang,Wang, Xiang,Wang, Nan,Peng, Tai,Wang, Suning
, p. 2677 - 2684 (2017)
A 1,1-hydroboration reaction was used successfully to create brominated BN-heterocyclic compounds, which are amenable to Stille coupling reactions for the construction of new BN-heterocyclic compounds, including a new polymeric BN-heterocycle that has an extended π-conjugated backbone. The conjugated backbone of the new BN-heterocycles was found to have a great influence on the photophysical and electronic properties of this class of compounds. In addition, the photoelimination reactivity of the new BN-heterocycles was also found to be greatly dependent on the extent of the conjugated backbone. Several new 1,2,4-triazole-fused boranaphthalenes have been obtained successfully via photoelimination.
Triazolo isoindole derivatives
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, (2008/06/13)
New s-triazolo[5,1-a]isoindole derivatives of following formula I STR1 wherein R is selected from hydrogen, amino, lower alkyl amino, di-lower alkyl amino, acylamino, diacylamino, benzoylamino, ureido, thioureido, carbethoxythioureido, benzoylthioureido,
