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Silyl Tosylate Precursors to Cyclohexyne, 1,2-Cyclohexadiene, and 1,2-Cycloheptadiene

Matthew McVeigh, Andrew V. Kelleghan, Michael M. Yamano, Rachel R. Knapp, Neil K. Garg

2020Organic Letters25 citationsDOIOpen Access PDF

Abstract

Transient strained cyclic intermediates have become valuable intermediates in modern synthetic chemistry. Although silyl triflate precursors to strained intermediates are most often employed, the instability of some silyl triflates warrants the development of alternative precursors. We report the syntheses of silyl tosylate precursors to cyclohexyne, 1,2-cyclohexadiene, and 1,2-cycloheptadiene. The resultant strained intermediates undergo trapping in situ to give cycloaddition products. Additionally, the results of competition experiments between silyl triflates and silyl tosylates are reported.

Topics & Concepts

SilylationTrifluoromethanesulfonateChemistryCycloadditionOrganic chemistryCatalysisCyclization and Aryne ChemistryAsymmetric Synthesis and CatalysisSynthetic Organic Chemistry Methods
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