Determination of the Rate Constant of the [4 + 2] Cycloaddition Between an Aryne Atropisomer and Furan in Solution
Author:
Affiliation:
1. Aix Marseille Univ, CNRS, Centrale Marseille, ISM2, Marseille, France
2. Aix Marseille Univ, CNRS, Centrale Marseille, FSCM, Marseille, France
Funder
Minist?re de l'Enseignement Sup?rieur et de la Recherche
Aix-Marseille Universit?
Centre National de la Recherche Scientifique
?cole centrale de Marseille
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01394
Reference44 articles.
1. Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds
2. Synthesis of Nanographenes, Starphenes, and Sterically Congested Polyarenes by Aryne Cyclotrimerization
3. Exploration of Kobayashi's aryne precursor: a potent reactive platform for the synthesis of polycyclic aromatic hydrocarbons
4. The Lowest Singlet and Triplet States ofo-Benzyne: Spin-Coupled Interpretation of the Electronic Structure at CAS SCF Equilibrium Geometries
5. Theoretical Studies of the Structure, Aromaticity, and Magnetic Properties ofo-Benzyne
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1. Asymmetric Cycloaddition Reactions of Aryne Intermediates with a Chiral Carbon–Carbon Axis: Syntheses of Axially Chiral Biaryl Compounds;Organic Letters;2023-12-06
2. Asymmetric reactions involving aryne intermediates;Nature Reviews Chemistry;2023-03-31
3. Aryne Atropisomers: Chiral Arynes for the Enantiospecific Synthesis of Atropisomers and Nanographene Atropisomers;Accounts of Chemical Research;2023-01-03
4. Enantiospecific Syntheses of Congested Atropisomers through Chiral Bis(aryne) Synthetic Equivalents;Chemistry – A European Journal;2022-09-29
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