A Catalytic Highly Enantioselective Synthesis of Spirooxazolines

25 May 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A catalytic highly enantioselective synthesis of spirooxazolines is presented. Starting from readily available 2-naphthol-substituted benzamides and using catalytic amounts of a chiral triazole-substituted iodoarene catalyst, a variety of spirooxazolines can be isolated through an enantioselective oxidative dearomatization in up to 92% yield and 97% ee. The further synthetic utility of the optically enriched spirooxazolines was examined providing a corresponding 2-naphthalenole and an oxepin.

Keywords

spirocyclization
enantioselective catalysis
spirooxazoline
hypervalent iodine oxidation

Supplementary materials

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TOC ChemRXIV
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Spirooxazolines Support ChemRXIV
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