Transition-metal-catalyzed regioselective aroyl- and trifluoro-acetylthiolation of alkynes using thioesters

Transition-metal-catalyzed regioselective aroyl- and trifluoro-acetylthiolation of alkynes using thioesters

Intermolecular CO-retained carbothiolation of alkynes using thioesters took place to afford beta-SR substituted enone derivatives; the choice of catalyst (Pd(dba)(2)-dppe) and the introduction of a CF(3) group into the thioesters are the key to achieving the transformation.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2009-01 (21), p.3080-3082
Hauptverfasser: Minami, Yasunori, Kuniyasu, Hitoshi, Miyafuji, Kiyoshi, Kambe, Nobuaki
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container_title Chemical communications (Cambridge, England)
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creator Minami, Yasunori
Kuniyasu, Hitoshi
Miyafuji, Kiyoshi
Kambe, Nobuaki
description Intermolecular CO-retained carbothiolation of alkynes using thioesters took place to afford beta-SR substituted enone derivatives; the choice of catalyst (Pd(dba)(2)-dppe) and the introduction of a CF(3) group into the thioesters are the key to achieving the transformation.
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title Transition-metal-catalyzed regioselective aroyl- and trifluoro-acetylthiolation of alkynes using thioesters
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