Reply to the ‘Comment on “trans-1,2-Disiloxybenzocyclobutene, an adequate partner for the auto-oxidation: EPR/spin trapping and theoretical studies”’ by H.-G. Korth, P. Mulder and T. Paul, Phys. Chem. Chem. Phys., 2017, 19, C6CP04187F
Author:
Affiliation:
1. Aix Marseille Univ
2. CNRS
3. Centrale Marseille
4. Marseille
5. France
6. ICR
Abstract
New insights were provided for the understanding of the reaction mechanism of the auto-oxidation of a trans-1,2-disiloxybenzocyclobutene.
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2017/CP/C6CP07923G
Reference16 articles.
1. trans-1,2-Disiloxybenzocyclobutene, an adequate partner for the auto-oxidation: EPR/spin trapping and theoretical studies
2. Dramatic influence of the substitution of alkylidene-5H-furan-2-ones in Diels–Alder cycloadditions with o-quinonedimethide as diene partner: en route to the CDEF polycyclic ring system of lactonamycin
3. Thermal Rearrangements of Di- and Triphenyl-Substituted Benzocyclobutenes and Correspondingo-Quinodimethanes
4. A Powerful o-Quinone Dimethide Strategy for Intermolecular Diels−Alder Cycloadditions
5. Algorithmic tools in the study of semiempirical potential surfaces
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