Synthesis and Reactivity of 23-tert-Butyl- and 23-Phenyltetraarylazuliporphyrins: an Analysis of the Effect of Bulky Substituents on Oxidative Ring Contractions to Benzocarbaporphyrins-Reference-Cited by-同舟云学术

Synthesis and Reactivity of 23-tert-Butyl- and 23-Phenyltetraarylazuliporphyrins: an Analysis of the Effect of Bulky Substituents on Oxidative Ring Contractions to Benzocarbaporphyrins

Published:2007-08 Issue:24 Volume:2007 Page:3981-3990
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

El-Beck Jessica A.,Lash Timothy D.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference32 articles.

1. Synthesis, Spectroscopy, and Reactivity of meso-Unsubstituted Azuliporphyrins and Their Heteroanalogues. Oxidative Ring Contractions to Carba-, Oxacarba-, Thiacarba-, and Selenacarbaporphyrins

2. Azuliporphyrin: Grenzfall eines aromatischen, porphyrinoiden Makrocyclus

3. Porphyrin Synthesis by the “3+1” Approach: New Applications for an Old Methodology

4. An Azulene Analogue of the Tripyrranes and Carbaporphyrinoids Therefrom Conjugated Macrocycles Related to the Porphyrins, Part 19. This work was supported by the National Science Foundation under Grant Nos. CHE-9732054 and CHE-0134472. Mass spectral determinations were made at the Mass Spectral Laboratory, School of Chemical Sciences, University of Illinois at Urbana-Champaign, supported in part by a grant from the National Institute of General Medical Sciences (GM 27029). Elemental analyses were obtained from the School of Chemical Sciences Microanalysis Laboratory at the University of Illinois. Part 18: ref. [1].

5. Synthesis of Sapphyrins, Heterosapphyrins, and Carbasapphyrins by a “4 + 1” Approach

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