80290-29-5Relevant articles and documents
Sulfur-mediated allylic C-H arylation, epoxidation, and aziridination
Luo, Hang,Hu, Gang,Li, Pingfan
, p. 10569 - 10578 (2019)
Transition-metal-free, sulfur-mediated allylic C-H arylation, epoxidation, and aziridination were realized through one-pot procedures. The reaction design involved initial addition between olefins and triflic anhydride activated sulfoxides, followed by subsequent reactions of the allylic sulfur ylides generated under basic conditions with arylboronic acids, aldehydes, or aldimines, to give allylic arylation, epoxidation, or aziridination products, respectively.
1,3-Bis(trimethylsilyl)propene as 1,3- and 3,3-Propene Dianion Synthons. Reactions of 2-Aryl-1,3-bis(trimethylsilyl)propenes with Electrophiles
Weng, Wu-Wang,Luh, Tien-Yau
, p. 2760 - 2762 (2007/10/02)
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