Sustainable radical approaches for cross electrophile coupling to synthesize trifluoromethyl- and allyl-substituted tert-alcohols
Muhammad Awais Ashraf, Yunjeong Lee, Naila Iqbal, Naeem Iqbal, Eun Jin Cho
Abstract
-alcohols. Reactions proceed through trifluoromethyl ketyl radical and allyl radical intermediates, which undergo challenging radical-radical cross-coupling. The developed transformations are mild and chemo-selective to give cross-coupled products and deliver a wide range of valuable trifluoromethyl- and allyl-containing tertiary alcohols. Both processes can also be applied for the synthesis of amine variant containing trifluoromethyl and allyl moiety, which is considered as amide bioisostere.
Topics & Concepts
TrifluoromethylChemistryMoietyElectrophileCombinatorial chemistryOrganic chemistryMedicinal chemistryAlkylCatalysisFluorine in Organic ChemistryRadical Photochemical ReactionsSulfur-Based Synthesis Techniques