4.7 Article

Mn(i) phosphine-amino-phosphinites: a highly modular class of pincer complexes for enantioselective transfer hydrogenation of aryl-alkyl ketones

Journal

DALTON TRANSACTIONS
Volume 50, Issue 40, Pages 14115-14119

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt02257a

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Funding

  1. Swiss National Science Foundation [200020_184606]
  2. Swiss National Science Foundation (SNF) [200020_184606] Funding Source: Swiss National Science Foundation (SNF)

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A series of Mn(i) catalysts with P'(O)N(H)P pincer ligands have been explored for the asymmetric transfer hydrogenation of aryl-alkyl ketones, leading to good to high enantioselectivities compared to other Mn-based catalysts for such reactions. The chiral backbone and phosphine moieties of P'(O)N(H)P make it an alternative ligand framework to the well-known PNP-type pincers.
A series of Mn(i) catalysts with readily accessible and more pi-accepting phosphine-amino-phosphinite (P '(O)N(H)P) pincer ligands have been explored for the asymmetric transfer hydrogenation of aryl-alkyl ketones which led to good to high enantioselectivities (up to 98%) compared to other reported Mn-based catalysts for such reactions. The easy tunability of the chiral backbone and the phosphine moieties makes P '(O)N(H)P an alternative ligand framework to the well-known PNP-type pincers.

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