Control of stereogenic oxygen in a helically chiral oxonium ion
Owen Smith,
Mihai V. Popescu,
Madeleine J. Hindson,
Robert S. Paton (),
Jonathan W. Burton () and
Martin D. Smith ()
Additional contact information
Owen Smith: University of Oxford
Mihai V. Popescu: University of Oxford
Madeleine J. Hindson: University of Oxford
Robert S. Paton: Colorado State University
Jonathan W. Burton: University of Oxford
Martin D. Smith: University of Oxford
Nature, 2023, vol. 615, issue 7952, 430-435
Abstract:
Abstract The control of tetrahedral carbon stereocentres remains a focus of modern synthetic chemistry and is enabled by their configurational stability. By contrast, trisubstituted nitrogen1, phosphorus2 and sulfur compounds3 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 intermediates5,6. 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 inversion7 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.
Date: 2023
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DOI: 10.1038/s41586-023-05719-z
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