Reactivity of Homoallylic Substituted Adamantylideneadamantanes with Bromine. Substituent Effects on the Stability of the Ionic and Nonionic Intermediates-Reference-Cited by-同舟云学术

Reactivity of Homoallylic Substituted Adamantylideneadamantanes with Bromine. Substituent Effects on the Stability of the Ionic and Nonionic Intermediates

Published:2002-09-10 Issue:20 Volume:67 Page:7066-7074
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chiappe Cinzia¹,Rubertis Antonietta De¹,Jaber Ali¹,Lenoir Dieter¹,Wattenbach Carsten¹,Pomelli Christian Silvio¹

Affiliation:

1. Dipartimento di Chimica Bioorganica e Biofarmacia, Università di Pisa, Via Bonanno 33, I-56126 Pisa, Italy, Institut für Ökologische Chemie, GSF-Forschungszentrum für Umwelt und Gesundheit, Postfach 1129, D-85778 Neuherberg bei München, Germany, Lehrstuhl für Chemisch-Technische Analyse und Chemische Lebensmitteltechnologie Weihenstephaner Steig 23 D-85350 Freising-Weihenstephan, Germany, and Dipartimento di Chimica e Chimica Industriale, Università di Pisa, via Risorgimento 35, I-56126 Pisa, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0203490

Reference32 articles.

1. (a) Schmid, G. H.The Chemistry of Double-Bonded Functionalgroups; Patai, S., Ed.; Wiley: New York, 1989; Suppl. A, Vol. 2, part 1, p 699.

2. Investigation of the Early Steps in Electrophilic Bromination through the Study of the Reaction with Sterically Encumbered Olefins

3. Functionalized Polymers-Emerging Versatile Tools for Solution-Phase Chemistry and Automated Parallel Synthesis

4. Investigation of the early stages of electrophilic addition of bromine to olefins. Kinetic evidence for a reversibly formed bromonium ion in the reaction of bromine with tetraisobutylethylene

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