Regio- and diastereoselective access to densely functionalized ketones <i>via</i> the Boekelheide rearrangement of isoxazoline <i>N</i>-oxides-Reference-Cited by-同舟云学术

Regio- and diastereoselective access to densely functionalized ketones via the Boekelheide rearrangement of isoxazoline N-oxides

Published:2022 Issue:28 Volume:20 Page:5624-5637
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Ushakov Pavel Yu.¹,Ioffe Sema L.¹,Sukhorukov Alexey Yu.¹^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, Russian Federation

Abstract

A “renewed isoxazoline route” toward densely functionalized ketones avoiding the use of unstable and hazardous nitrile oxide intermediates has been developed.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB00787H

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