Pd-Catalyzed sequential B(3)-I/B(4)-H bond activation for the synthesis of 3,4-benzo--carboranes.

Dalton Trans

Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Rd, Shanghai 200032, China. and Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, N. T., Hong Kong, China.

Published: February 2021

A palladium-catalyzed sequential B(3)-I and B(4)-H bond activation has been achieved for the synthesis of 3,4-benzo-o-carboranes via a formal [2 + 2 + 2] cycloaddition of 3-I-o-carborane with 2 equiv. of arylalkynes. This represents a new protocol to construct o-carborane-fused cyclics in one process, in which the Pd fragment migrates formally from the B(3) to B(4) position of the cage.

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Source
http://dx.doi.org/10.1039/d0dt03740kDOI Listing

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