Unusual reactivity of rhodium carbenes with allenes: An efficient asymmetric synthesis of methylenetetrahydropyran scaffolds

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Abstract

A RhI/(S)-BINAP catalytic system is able to promote carbene alkyne metathesis and cascade this elemental step with an stereoselective reaction with allenes. An unusual carbene/allene reactivity is discovered that, through a formal addition of p-toluenesulfinic acid to a Rh-bound trimethylenemethane intermediate, affords 4-methylenetetrahydropyran compounds in good yields and excellent enantioselectivities.

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Torres, Ò., Solà, M., Roglans, A., & Pla-Quintana, A. (2017). Unusual reactivity of rhodium carbenes with allenes: An efficient asymmetric synthesis of methylenetetrahydropyran scaffolds. Chemical Communications, 53(71), 9922–9925. https://doi.org/10.1039/c7cc04803c

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