Neue Homobenzvalen‐Derivate (Tricyclo[4.1.0.0 2,7 ]hept‐3‐ene)
Author:
Affiliation:
1. Institut für Organische Chemie der Universität Würzburg, Am Hubland, D‐8700 Würzburg
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19861190114
Reference49 articles.
1. The consequences of methyl substitution on the efficiency and regioselectivity of C-H insertion during intramolecular cyclization of norcaran-7-, 3-norcaren-7-, and tricyclo[5.1.0.03,5]octan-8-ylidenes
2. Electronic structure of tricyclo[4.1.0.02,7]hept-3-enes. Correlation with the regioselectivity of electrophilic attack
3. Cycloaddition reactions of triazolinediones to tricyclo[4.1.0.02,7]hept-3-enes. Consequences of charge control as compared to frontier orbital control
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4. Solvolysis of Tricyclo[4.1.0.02,7]hept-4-en-3-yl and Tricyclo[4.1.0.02,7]hept-3-yl Methanesulfonates andp-Nitrobenzoates – Remarkably Small Enthalpy Difference between the C7H7 Cations Tricyclo[4.1.0.02,7]hept-4-en-3-yl and 7-Norbornadienyl;Liebigs Annalen;1997-01
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