Accessing Two-Stage Regioselective Photoisomerization in Unsymmetrical N,C-Chelate Organoboron Compounds: Reactivity of B(ppz)(Mes)Ar
收藏Figshare2018-09-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Accessing_Two-Stage_Regioselective_Photoisomerization_in_Unsymmetrical_N_C-Chelate_Organoboron_Compounds_Reactivity_of_B_ppz_Mes_Ar/7115456
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A new family of unsymmetrical, N,C-chelate organoboron compounds B(ppz)(Mes)Ar have been synthesized and found to undergo a rare, regioselective two-stage photoisomerization, involving the Ar group only. The initial transformation is a Zimmerman rearrangement to afford yellow azaboratabisnorcaradiene isomers that are subsequently converted to unprecedented 14aH-diazaborepins via a photochemical “walk” rearrangement. Spectroscopic and computational studies provide insight into the formation and properties of these unique systems.
创建时间:
2018-09-20



