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・ Thiotricha crypsichlora
・ Thiotricha cuneiformis
・ Thiotricha delacma
・ Thiotricha dissobola
・ Thiotricha embolarcha
・ Thiotricha epiclista
・ Thiotricha eremita
・ Thiotricha flagellatrix
・ Thiotricha fridaella
・ Thiotricha fusca
・ Thiotricha galactaea
・ Thiotricha galenaea
・ Thiol S-methyltransferase
・ Thiol sulfotransferase
・ Thiol-activated cytolysin
Thiol-ene reaction
・ Thiol-yne reaction
・ Thiolactic acid
・ Thiolactone
・ Thiolase
・ Thiolate-protected gold cluster
・ Thiolières
・ Thiolutin
・ Thiolysis
・ Thiolyte
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・ Thiomargarita namibiensis
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Thiol-ene reaction : ウィキペディア英語版
Thiol-ene reaction

The thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol and an alkene to form an alkyl sulfide. This reaction was first reported in 1905, but it gained prominence in the late 1990s and early 2000s for its feasibility and wide range of applications.〔Lowe, A. B. ''Polymer Chemistry'' 2010, 1 (1), 17–36. DOI: (10.1039/B9PY00216B )〕〔Nilsson, C.; Simpson, N.; Malkoch, M.; Johansson, M.; Malmstrom, E. ''Journal of Polymer Science: Part A: Polymer Chemistry'' 2008, 46, 1339-1348. DOI: (1002/pola.22474 )〕 This reaction is accepted as a click chemistry reaction given the reactions’ high yield, stereoselectivity, high rate, and thermodynamic driving force.
The reaction results in a anti-Markovnikov addition of a thiol compound to an alkene. Given the stereoselectivity, high rate and yields, this reaction is synthetically useful for organic chemists. Thiol-ene reactions have numerous applications in material and biomedical sciences.〔〔Hoyle, C. E.; Bowman, C. N. ''Agewandte Chemie International Edition'' 2010, 49 (9), 1540–1573. DOI: (10.1002/anie.200903924 )〕
==Mechanisms==


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