Oxidant mediated coupling of tetrapyrromethanes resulted in the exclusive formation of meso-substituted corroles in more than 60% yields. The similar coupling reaction of 1,14-unsubstituted 16-oxatripyrromethane with 5-tolyldipyrromethane carried out in acetonitrile also gave expanded corroles as a
ChemInform Abstract: Expedient Synthesis of Corroles by Oxidant-Mediated, Direct .alpha±alpha.′ Coupling of Tetrapyrromethanes.
✍ Scribed by Jae-Won Ka; Won-Seob Cho; Chang-Hee Lee
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 33 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
📜 SIMILAR VOLUMES
Novel Concepts in Directed Biaryl Synthesis. Part 76. First Synthesis of Mastigophorenes A and B, by Biomimetic Oxidative Coupling of Herbertenediol. -The first synthesis of the title compounds (I), which are atropisomers, by oxidative phenolic coupling of partially protected derivatives of their j