Asymmetric Organocatalyzed Synthesis of α‐Aminophosphinates via Thiourea Anion‐Binding Catalysis

Author:

Niland Cáoimhe J.1,Ruddy Joseph J.2,O’Fearraigh Martin P.2,McGarrigle Eoghan M3

Affiliation:

1. An Coláiste Ollscoile Baile Átha Cliath SSPC, the SFI Research Centre for Pharmaceuticals, Centre for Synthesis & Chemical Biology, UCD School of Chemistry IRELAND

2. An Coláiste Ollscoile Baile Átha Cliath Centre for Synthesis & Chemical Biology, UCD School of Chemistry IRELAND

3. University College Dublin - National University of Ireland: University College Dublin UCD School of Chemistry Centre for Synthesis & Chemical Biology UCD School of Chemistry Belfield 4 Dublin IRELAND

Abstract

Thioureas catalyze the reaction of phosphonites with in situ‐generated isoquinolinium salts to give C and P‐stereogenic α‐aminophosphinates in high enantioselectivity (up to 96%) and yield (up to 95%). Low diastereoselectivity was obtained and this is rationalized in the context of a mechanistic proposal involving anion‐binding catalysis of the P‐C bond formation step followed by uncatalyzed Arbuzov collapse. The scope of the reaction, including a g‐scale example, was demonstrated.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

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