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Published October 28, 2020 | Published + Supplemental Material
Journal Article Open

Enantioselective synthesis of highly oxygenated acyclic quaternary center-containing building blocks via palladium-catalyzed decarboxylative allylic alkylation of cyclic siloxyketones

Abstract

The development of a palladium-catalyzed enantioselective decarboxylative allylic alkylation of cyclic siloxyketones to produce enantioenriched silicon-tethered heterocycles is reported. The reaction proceeds smoothly to provide products bearing a quaternary stereocenter in excellent yields (up to 91% yield) with high levels of enantioselectivity (up to 94% ee). We further utilized the unique reactivity of the siloxy functionality to access chiral, highly oxygenated acyclic quaternary building blocks. In addition, we subsequently demonstrated the utility of these compounds through the synthesis of a lactone bearing vicinal quaternary-trisubstituted stereocenters.

Additional Information

This journal is © The Royal Society of Chemistry 2020. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. Received 9th August 2020. Accepted 10th September 2020. The NIH-NIGMS (R01GM080269) and Caltech are thanked for support of our research program. A. N. thanks the Royal Thai Government Scholarship program. T. I. thanks Japan Tobacco Inc. for funding. We thank Dr Makoto Shiozaki for helpful discussion and Dr Mona Shahgholi for mass spectrometry assistant. Dr Scott Virgil is acknowledged for instrumentation and SFC assistance. A. N. and T. I. contributed equally to this work. All publication charges for this article have been paid for by the Royal Society of Chemistry.

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Created:
August 19, 2023
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