Rational selection of co-catalysts for the deaminative hydrogenation of amides.

ABSTRACT: The catalytic hydrogenation of amides is an atom economical method to synthesize amines. Previously, it was serendipitously discovered that the combination of a secondary amide co-catalyst with (^iPrPNP)Fe(H)(CO) (^iPrPNP = N[CH₂CH₂(PⁱPr₂)]₂ ^-), results in a highly active base metal system for deaminative amide hydrogenation. Here, we use DFT to develop an improved co-catalyst for amide hydrogenation. Initially, we computationally evaluated the ability of a series of co-catalysts to accelerate the turnover-limiting proton transfer during C-N bond cleavage and poison the (^iPrPNP)Fe(H)(CO) catalyst through a side reaction. TBD (triazabicyclodecene) was identified as the leading co-catalyst. It wa

SUBMITTER: Artus Suarez L 

PROVIDER: S-EPMC7059200 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature