The Thermal Retro[2+2+2]cycloaddition of Cyclohexane Activated by Triscyclobutenannelation: Concerted All-Disrotatory versus Stepwise Conrotatory Pathways to Fused [12]Annulenes-Reference-Cited by-同舟云学术

The Thermal Retro[2+2+2]cycloaddition of Cyclohexane Activated by Triscyclobutenannelation: Concerted All-Disrotatory versus Stepwise Conrotatory Pathways to Fused [12]Annulenes

Published:2007-09-10 Issue:36 Volume:46 Page:6894-6898
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Eichberg Michael J.,Houk K. N.,Lehmann Jürg,Leonard Philip W.,Märker Anne,Norton Joseph E.,Sawicka Dorota,Vollhardt K. Peter C.,Whitener Glenn D.,Wolff Stefan

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference46 articles.

1. Carbocyliccis-[1.1.1]-Tris-σ-homobenzenes – Syntheses by Triple Epoxide → Cyclopropane Conversions, Structural Data, [σ2s+σ2s+σ2s] Cycloreversions

2. A cyclic trimer of perfluorocyclobutadiene

3. Three-Membered-Ring-Based Molecular Architectures

4. Preparation and Properties of Centrally Bridgehead-Substituted Hexacyclo[4.4.0.02,1.03,5.04,8.07,9]decanes (“Diademanes”) and Related (CH)10 Hydrocarbons

5. Aromaticity and Antiaromaticity in Small Ring Transition States, Assessed by NICS Values and Energetics

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