Unveiling the mechanism and regioselectivity of the [3 + 2] cycloaddition reaction between N-methylphenylnitrone and 1-sulphonyl-1-trifluoromethylallene. A MEDT study-Reference-Cited by-同舟云学术

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Unveiling the mechanism and regioselectivity of the [3 + 2] cycloaddition reaction between N-methylphenylnitrone and 1-sulphonyl-1-trifluoromethylallene. A MEDT study

Published:2024-02-02 Issue:17 Volume:122 Page:
ISSN:0026-8976
Container-title:Molecular Physics
language:en
Short-container-title:Molecular Physics

Author:

Messikh Samia¹,Sobhi Chafia¹^ORCID,Malfi Najran¹^ORCID,Yahia Wassila²,Chouit Hanifa¹,Kerboua Adlen¹,Chermette Henry³^ORCID

Affiliation:

1. Laboratory of Materials and Energetic Engineering, Faculty of Technology, University 20 August 1955 Skikda, Skikda, Algeria

2. Laboratoire Physico-Chimie Des Surfaces Et Interfaces, University 20 August 1955 Skikda, Skikda, Algeria

3. Université Claude Bernard Lyon 1, Institut des Sciences Analytiques, Université de Lyon, Lyon, France

Funder

Ministry of Higher Education and Scientific Research of the Algerian Government

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/00268976.2024.2308679

Reference58 articles.

1. N. Nishiwaki (ed.), Methods and Applications of Cycloaddition Reactions in Organic Syntheses (John Wiley & Sons, 2013).

2. S. Kobayashi and K.A. Jorgensen, Cycloaddition Reactions in Organic Synthesis (John Wiley & Sons, 2002).

3. 1,3-Dipolar Cycloadditions. Past and Future

4. A. Padwa and W.H. Pearson (ed.), Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles And Natural Products (John Wiley & Sons, 2003).

5. A. Padwa, 1,3 Dipolar Cycloaddition Chemistry (John Wiley & Sons, New York, 1984).

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