Arylallenes and the halogeno-B(C6F5)2 reagents: facile formation of 2-borylindenes

Tao, X.; Daniliuc, C. G.; Soloviova, K.; Strassert, C. A.; Kehr, G.; Erker, G.

Research article (journal) | Peer reviewed

Abstract

Phenylallene reacts rapidly with ClB(C6F5)2 to give the respective 2-borylindene. Several substituted allenylarenes form the respective 2-B(C6F5)2 boryl-substituted indenes upon treatment with ClB(C6F5)2 or BrB(C6F5)2 as well. Bis- and tris-allenylarenes form the corresponding products featuring multiple five-membered ring annulations{,} including a symmetrical tris-borylated dihydro-1H-trindene derivative. The B(C6F5)2 borylindenes show fluorescence properties.

Details about the publication

JournalChemical communications (Chem. Commun.)
Volume55
Page range10166-10169
StatusPublished
Release year2019
Language in which the publication is writtenEnglish
DOI10.1039/C9CC04199K
Link to the full texthttp://dx.doi.org/10.1039/C9CC04199K
KeywordsPhenylallene; boryl-substituted; fluorescence

Authors from the University of Münster

Strassert, Cristian
Professoship for Coordination Chemistry and Functional Imaging