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Synthesis method unlocks a pathway to valuable fluorinated drug compounds for new medicinesThe resulting copper difluorocarbenoid complex coordinates with the epoxide and triggers site-selective ring cleavage and cyclization, to yield the desired α,α-difluoro-oxetane product via a ...
The resulting copper difluorocarbenoid complex coordinates with the epoxide and triggers site-selective ring cleavage and cyclisation, to yield the desired α,α-difluoro-oxetane product via a ...
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