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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693942PMC
http://dx.doi.org/10.1021/jacs.9b06277DOI Listing

Publication Analysis

Top Keywords

annulation amines
8
amines carboxylic
8
carboxylic acids
8
c-n c-c
8
p/p redox
8
redox catalysis
8
driving recursive
4
recursive dehydration
4
p/p
4
dehydration p/p
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!