Diels−Alder Reactions of Masked o-Benzoquinones:  New Experimental Findings and a Theoretical Study of the Inverse Electron Demand Case

Diels−Alder Reactions of Masked o-Benzoquinones:  New Experimental Findings and a Theoretical Study of the Inverse Electron Demand Case

Diels−Alder reactions of the masked o-benzoquinone (MOB) 2 with vinylene carbonate (3), the bicyclic derivatives 4, 5, and 6, and the intramolecular version of the 2-hydroxymethylfuran-MOB Diels−Alder reaction are described. In addition, a theoretical study of the Diels−Alder reactions of MOBs with...

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Veröffentlicht in:Journal of organic chemistry 2004-04, Vol.69 (7), p.2348-2354
Hauptverfasser: Arjona, Odón, Medel, Rocío, Plumet, Joaquín, Herrera, Rafael, Jiménez-Vázquez, Hugo A, Tamariz, Joaquín
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Chemistry
Exact sciences and technology
Kinetics and mechanisms
Organic chemistry
Reactivity and mechanisms
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container_end_page 2354
container_issue 7
container_start_page 2348
container_title Journal of organic chemistry
container_volume 69
creator Arjona, Odón
Medel, Rocío
Plumet, Joaquín
Herrera, Rafael
Jiménez-Vázquez, Hugo A
Tamariz, Joaquín
description Diels−Alder reactions of the masked o-benzoquinone (MOB) 2 with vinylene carbonate (3), the bicyclic derivatives 4, 5, and 6, and the intramolecular version of the 2-hydroxymethylfuran-MOB Diels−Alder reaction are described. In addition, a theoretical study of the Diels−Alder reactions of MOBs with enol and thioenol ethers is presented.
doi_str_mv 10.1021/jo030307r
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subjects Chemistry
Exact sciences and technology
Kinetics and mechanisms
Organic chemistry
Reactivity and mechanisms
title Diels−Alder Reactions of Masked o-Benzoquinones:  New Experimental Findings and a Theoretical Study of the Inverse Electron Demand Case
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