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a raises questions about a mechanism involving a hydration of the triple bond followed by the elimination of water. As our catalytic system shows with terminal alkynes only poor to moderate conversions into the Meyer-Schuster products, we suggest under our reaction conditions a different reactivity of terminal alkynes compared to internal alkynes. For the observation of such a dichotomy, see: 10.1021/ja809403e
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a raises questions about a mechanism involving a hydration of the triple bond followed by the elimination of water. As our catalytic system shows with terminal alkynes only poor to moderate conversions into the Meyer-Schuster products, we suggest under our reaction conditions a different reactivity of terminal alkynes compared to internal alkynes. For the observation of such a dichotomy, see:. Marion N., Rámon R.S., and Nolan S.P. J. Am. Chem. Soc. 131 (2009) 10.1021/ja809403e
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