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Bootwicha, Teerawut, Liu, Xiangqian, Pluta, Roman, Atodiresei, Iuliana, Rueping, Magnus (2013) N-Trifluormethylthiophthalimid: ein stabiles, elektrophiles SCF3- Reagens und seine Anwendung in der katalytischen asymmetrischen Trifluormethylsulfenylierung. Angewandte Chemie, 125 (49). 13093-13097 doi:10.1002/ange.201304957

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Reference TypeJournal (article/letter/editorial)
TitleN-Trifluormethylthiophthalimid: ein stabiles, elektrophiles SCF3- Reagens und seine Anwendung in der katalytischen asymmetrischen Trifluormethylsulfenylierung
JournalAngewandte Chemie
AuthorsBootwicha, TeerawutAuthor
Liu, XiangqianAuthor
Pluta, RomanAuthor
Atodiresei, IulianaAuthor
Rueping, MagnusAuthor
Year2013 (December 2)Volume125
Issue49
PublisherWiley
DOIdoi:10.1002/ange.201304957Search in ResearchGate
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Mindat Ref. ID7323611Long-form Identifiermindat:1:5:7323611:7
GUID0
Full ReferenceBootwicha, Teerawut, Liu, Xiangqian, Pluta, Roman, Atodiresei, Iuliana, Rueping, Magnus (2013) N-Trifluormethylthiophthalimid: ein stabiles, elektrophiles SCF3- Reagens und seine Anwendung in der katalytischen asymmetrischen Trifluormethylsulfenylierung. Angewandte Chemie, 125 (49). 13093-13097 doi:10.1002/ange.201304957
Plain TextBootwicha, Teerawut, Liu, Xiangqian, Pluta, Roman, Atodiresei, Iuliana, Rueping, Magnus (2013) N-Trifluormethylthiophthalimid: ein stabiles, elektrophiles SCF3- Reagens und seine Anwendung in der katalytischen asymmetrischen Trifluormethylsulfenylierung. Angewandte Chemie, 125 (49). 13093-13097 doi:10.1002/ange.201304957
In(2013, December) Angewandte Chemie Vol. 125 (49) Wiley

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Bootwicha, Teerawut, Liu, Xiangqian, Pluta, Roman, Atodiresei, Iuliana, Rueping, Magnus (2013) N-Trifluoromethylthiophthalimide: A Stable Electrophilic SCF3-Reagent and its Application in the Catalytic Asymmetric Trifluoromethylsulfenylation. Angewandte Chemie International Edition, 52 (49). 12856-12859 doi:10.1002/anie.201304957
Rueping, Magnus, Liu, Xiangqian, Bootwicha, Teerawut, Pluta, Roman, Merkens, Carina (2014) Catalytic enantioselective trifluoromethylthiolation of oxindoles using shelf-stable N-(trifluoromethylthio)phthalimide and a cinchona alkaloid catalyst. Chemical Communications, 50 (19). 2508pp. doi:10.1039/c3cc49877h
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