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Formal Addition of Acetone to Unactivated Michael Acceptors via Ring-Opening and Fragmentation of Dihydropyranones.pdf (899.67 kB)
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Formal Addition of Acetone to Unactivated Michael Acceptors via Ring-Opening and Retro-Claisen Fragmentation of Dihydropyranones

preprint
submitted on 13.09.2019 and posted on 16.09.2019 by Anton Axelsson, Emmelie Hammarvid, Martin Rahm, Henrik Sundén

We present a general protocol for the formal Michael addition of acetone to a,b-unsaturated esters and amides, a transformation difficult to perform using current methods. The protocol comprises of an amidine catalyzed relay ring-opening and fragmentation of 3,4-dihydropyranones. The reaction proceeds under mild conditions, has a broad substrate scope and the products can be isolated in good to excellent yields (30 examples, with up to 97 % yield). The method can be applied to homochiral substrates with total preservation of chiral information, generating products in high optical purity. Kinetic experiments upported by quantum chemical modeling indicates that the reaction is of second order with respect to the catalyst. The kinetic isotope effect has been determined to be 2.3, which supports a mechanism in which the catalyst takes a bifunctional role, acting both as a Brønsted base and as a hydrogen bond donor. The findings presented here enables a rapid entry to compounds previously considered difficult to access and highlights the dual functionality of amidine superbases as catalysts.

History

Email Address of Submitting Author

sundenh@chalmers.se

Institution

Chalmers University of Technology

Country

Sweden

ORCID For Submitting Author

0000-0001-6202-7557

Declaration of Conflict of Interest

The Authors declare no conflict of interest.

Version Notes

version numero uno

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