A three-component [3 + 2]-cycloaddition/elimination cascade for the synthesis of spirooxindole-pyrrolizines-Reference-Cited by-同舟云学术

A three-component [3 + 2]-cycloaddition/elimination cascade for the synthesis of spirooxindole-pyrrolizines

Published:2021 Issue:3 Volume:19 Page:667-676
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Palomba Martina¹²³⁴⁵,De Monte Emanuela¹²³⁴⁵,Mambrini Andrea¹²³⁴⁵,Bagnoli Luana¹²³⁴⁵^ORCID,Santi Claudio¹²³⁴⁵^ORCID,Marini Francesca¹²³⁴⁵^ORCID

Affiliation:

1. Department of Pharmaceutical Sciences (Group of Catalysis

2. Synthesis and Organic Green Chemistry)

3. University of Perugia

4. 1 – 06123 Perugia

5. Italy

Abstract

A three-component reaction of secondary α-aminoacids, isatins and vinyl selenones generated spirooxindole-tetrahydropyrrolizines via a [3 + 2]-cycloaddition/elimination cascade process.

Funder

Università degli Studi di Perugia

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02321C

Reference68 articles.

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4. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis

5. Current Trends towards the Synthesis of Bioactive Heterocycles and Natural Products Using 1,3-Dipolar Cycloadditions (1,3-DC) with Azomethine Ylides

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