An Experimental and Computational Study about the Effect of a Spirocyclopropane Group on the Solvolysis Rates of Bridgehead Triflates-Reference-Cited by-同舟云学术

An Experimental and Computational Study about the Effect of a Spirocyclopropane Group on the Solvolysis Rates of Bridgehead Triflates

Published:1999-07-01 Issue:15 Volume:64 Page:5611-5619
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Martínez Antonio García¹,Vilar Enrique Teso¹,de la Moya Cerero Santiago¹,Barcina José Osío¹,Pedro C. Gómez ¹

Affiliation:

1. Departamento de Química Orgánica I, Facultad de Ciencias Químicas, Universidad Complutense de Madrid (UCM), Ciudad Universitaria s/n, E-28040 Madrid, Spain, Departamento de Química Orgánica y Biología, Facultad de Ciencias, Universidad Nacional de Educación a Distancia (UNED), Senda del Rey s/n, E-28040 Madrid, Spain, Departamento de Química Física I, Facultad de Ciencias Químicas, Universidad Complutense de Madrid (UCM), Ciudad Universitaria s/n, E-28040 Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990701i

Reference61 articles.

1. New Carbocations—From Physical Organic Chemistry to Biochemistry

2. Low-temperature carbon-13 nuclear magnetic resonance spectroscopic investigation of C4H7+. Evidence for an equilibrium involving the nonclassical bicyclobutonium ion and the bisected cyclopropylcarbinyl cation

3. Nuclear magnetic double resonance studies of the dimethylcyclopropylcarbinyl cation. Measurement of the rotation barrier

4. Nortricyclylcarbinyl carbocations. Structural hybrides of cyclopropylcarbinyl and bridged 2-norbornyl carbocations

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