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Merck
  • A regioselective synthesis of poly-substituted aryl triflones through self-promoting three component reaction.

A regioselective synthesis of poly-substituted aryl triflones through self-promoting three component reaction.

Chemical communications (Cambridge, England) (2011-05-25)
Hikaru Yanai, Masaya Fujita, Takeo Taguchi
摘要

In the absence of any additional catalysts, the reactions of (CF(3)SO)(2)CH(2), aldehydes, and 1,3-dienes gave gem-bis(triflyl)cyclohexenes in excellent yields with high regioselectivity. gem-Bis(triflyl)cyclohexene products can be easily converted to the corresponding aryl trifluoromethyl sulfones.

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Sigma-Aldrich
环己烯, inhibitor-free, ReagentPlus®, 99%
Supelco
环己烯, analytical standard, ≥99.5% (GC)
Sigma-Aldrich
环己烯, contains 100 ppm BHT as inhibitor, ≥99.0%