Events The 8th International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

10.3390/ecsoc-8-01945

This submission belongs to the session a. General Organic Synthesis of the event The 8th International Electronic Conference on Synthetic Organic Chemistry

Published date

01 Nov, 2004

Citation

Davor Margetić, Ronald N. Warrener, David A. Mann, Douglas N. Butler, Zhi-Long Chen, Dipolarophylic Properties of 5,10,15,20-tetra-(3,5-di(tert-butyl)phenyl)porphyrin-2,3-dione, in Proceedings of The 8th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2004, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-8-01945

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Dipolarophylic Properties of 5,10,15,20-tetra-(3,5-di(tert-butyl)phenyl)porphyrin-2,3-dione

Davor Margetić ¹

Ronald N. Warrener ²

David A. Mann ²

Douglas N. Butler ²

Zhi-Long Chen ³

1. Laboratory for Physical Organic Chemistry, Department of Organic Chemistry and Biochemistry, Ruder Boškovic Institute, Bijenicka c. 54, 10000 Zagreb, Croatia

2. Intelligent Polymer Research Institute, University of Wollongong, Northfields Avenue, Wollongong, NSW, 2522, Australia

3. Leverhulmer Center for Innovative Catalysis, Department of Chemistry, The University of Liverpool, Liverpool L69 7ZD, UK

Abstract

In this paper we describe 1,3-dipolar cycloaddition reactions of 5,10,15,20-tetra-(3,5-di(tert-butyl)phenyl)porphyrin-2,3-dione with acetylene cyclobutene epoxide. This reaction offers new synthetic approach to formation of dyads having functional group at each termini of policyclic rigid framework.

Keywords

n/a

Intramolecular 1,3-dipolar Cycloreversion - A Key Step in Novel Thermal Isomerisations of Cyclobutane Di-(carbomethoxy) Triazolines

High Pressure Assisted Synthesis of Fused Norbornenes Containing Two 7-Metallonorbornene Units