New reagent space and new scope for the Castagnoli–Cushman reaction of oximes and 3-arylglutaconic anhydrides-Reference-Cited by-同舟云学术

New reagent space and new scope for the Castagnoli–Cushman reaction of oximes and 3-arylglutaconic anhydrides

Published:2022 Issue:44 Volume:20 Page:8643-8648
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Bannykh Anton¹,Levashova Ekaterina¹,Bakulina Olga¹,Krasavin Mikhail¹²^ORCID

Affiliation:

1. Saint Petersburg State University, Saint Petersburg 199034, Russian Federation

2. Immanuel Kant Baltic Federal University, Kaliningrad 236016, Russian Federation

Abstract

The Castagnoli–Cushman reaction of oximes, previously known only for homophthalic anhydride, was extended to 3-arylglutaconic anhydrides to produce a new family of cyclic hydroxamic acids from a significantly improved diversity of oxime substrates.

Funder

Russian Science Foundation

Russian Foundation for Basic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01675C

Reference24 articles.

1. Mechanistic Investigation of Castagnoli–Cushman Multicomponent Reactions Leading to a Three-Component Synthesis of Dihydroisoquinolones

2. Current diversity of cyclic anhydrides for the Castagnoli–Cushman-type formal cycloaddition reactions: prospects and challenges

3. A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline

4. Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction

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