A method for the annulation of amines and carboxylic acids to form pharmaceutically relevant azaheterocycles via organophosphorus P/P redox catalysis is reported. The method employs a phosphetane catalyst together with a mild bromenium oxidant and terminal hydrosilane reductant to drive successive C-N and C-C bond-forming dehydration events via the serial action of a catalytic bromophosphonium intermediate. These results demonstrate the capacity of P/P redox catalysis to enable iterative redox-neutral transformations in complement to the common reductive driving force of the P/P couple.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693942 | PMC |
http://dx.doi.org/10.1021/jacs.9b06277 | DOI Listing |
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