2° SEMINARIO QUÍMICA ORGÁNICA IQUIR 2023

SEMINARIO QUÍMICA ORGÁNICA 10-04-23

EXPOSITOR: Lic. Lucas Passaglia

TÍTULO: "Control of stereogenic oxygen in a helically chiral oxonium ion".

FUENTE: Smith, O., Popescu, M.V., Hindson, M.J., Paton, R.S, Burton, J.W., Smith M.D, Nature, 2023, 615, 430–435. https://doi.org/10.1038/s41586-023-05719-z

DÍA, HORA y LUGAR: Lunes 10 de abril de 2023, 14:00 h, Aula 18

Modalidad virtual, Link: meet.google.com/hjn-ygro-twf (Plataforma MEET GOOGLE)

RESUMEN: The control of tetrahedral carbon stereocentres remains a focus of modern synthetic chemistry and is enabled by their configurational stability. By contrast, trisubstituted nitrogen, phosphorus and sulfur compounds undergo pyramidal inversion, a fundamental and well-recognized stereochemical phenomenon that is widely exploited4. However, the stereochemistry of oxonium ions—compounds bearing three substituents on a positively charged oxygen atom—is poorly developed and there are few applications of oxonium ions in synthesis beyond their existence as reactive intermediates. There are no examples of configurationally stable oxonium ions in which the oxygen atom is the sole stereogenic centre, probably owing to the low barrier to oxygen pyramidal inversion and the perception that all oxonium ions are highly reactive. Here we describe the design, synthesis and characterization of a helically chiral triaryloxonium ion in which inversion of the oxygen lone pair is prevented through geometric restriction to enable it to function as a determinant of configuration. A combined synthesis and quantum calculation approach delineates design principles that enable configurationally stable and room-temperature isolable salts to be generated. We show that the barrier to inversion is greater than 110 kJ mol−1 and outline processes for resolution. This constitutes, to our knowledge, the only example of a chiral non-racemic and configurationally stable molecule in which the oxygen atom is the sole stereogenic centre.