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Mechanistic Insight from Lewis-Acid-Dependent Selectivity and Reversible Haloboration, as Harnessed for Boron-Based
Martin Stang1, Robert J Mycka1,2, Suzanne A Blum1
1Department of Chemistry, University of California, Irvine, California 92697-2025, United States.
Abstract:
Different reaction selectivity occurs with the Lewis acids B-chlorocatecholborane (ClBcat), B-bromocatecholborane (BrBcat), and BBr3, favoring either alkyne haloboration, electrophilic cyclization of a tethered nucleophilic sulfur onto the alkyne, or group transfer of the nucleophile. This reaction selectivity also depends on the chain length of the tethered nucleophile, revealing a subtle interplay of relative kinetics and thermodynamics. In all cases, BBr3 reacts readily with alkynes to form haloborated products; however, this process is reversible, and this reversibility can be harnessed to ultimately access regio- and stereodefined cyclic sulfonium zwitterions via the slower but thermodynamically favored electrophilic cyclization pathway. Reversibility was noted by following the reaction by NMR spectroscopy, and by characterizing the kinetic and thermodynamic products by a combination of 2D NMR spectroscopy and single-crystal X-ray diffraction. The "mixed" reagent bromocatechol borane (BrBcat) displayed reactivity between ClBcat and BBr3, producing bromoboration in some cases and electrophilic cyclization in others. With this enhanced understanding of the reaction dynamics, it becomes possible to use boron Lewis acids in a predictable manner in cases where haloboration is the kinetic product but in which the reversibility of this reaction maintains access to eventual alternative reactivity leading to desired building blocks in organic synthesis.
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