1174209-75-6Relevant academic research and scientific papers
Use of 1-pentafluorosulfanyl-phenylacetylenes for the preparation of SF5-substituted five-membered ring heterocycles through 1,3-dipolar cycloadditions. Isoxazoles and isoxazolines
Lopez, Simon E.,Mitani, Akira,Pena, Priscila,Ghiviriga, Ion,Dolbier, William R.
, p. 121 - 126 (2015/07/07)
Abstract A synthetic methodology utilizing 1,3-dipolar cycloadditions was developed for the preparation of pentafluorosulfanyl-substituted heterocycles using SF5-substituted arylacetylenes as key building block dipolarophiles. A group of 4-SFs
PREPARATION OF PENTAFLUOROSULFANYL (SF5) HETEROCYCLES: PYRROLES AND THIOPHENES
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Page/Page column 6, (2011/04/14)
The subject invention pertains to pentafluorosulfonyl (SF5) substituted pyrroles, thiophenes, 3-pyrrolines and 2,5-dihydrothiophenes, as well as methods for their synthesis.
Preparation of pentafluorosulfanyl (SF5) pyrrole carboxylic acid esters
Dolbier Jr., William R.,Zheng, Zhaoyun
experimental part, p. 5626 - 5628 (2009/12/08)
(Chemical Equation Presented) Pyrrole derivatives bearing a pentafluorosulfanyl group are currently unknown. In this paper, a facile preparation of SF5-substituted pyrrole carboxylic acid esters in good yield is reported. Utilizing the cycloadd
