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meso-Aryl-Substituted [26]Hexaphyrin(1.1.0.1.1.0) and [38]Nonaphyrin(1.1.0.1.1.0.1.1.0) from Oxidative Coupling of a Tripyrrane

✍ Scribed by Soji Shimizu; Ryuichiro Taniguchi; Atsuhiro Osuka

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
208 KB
Volume
117
Category
Article
ISSN
0044-8249

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📜 SIMILAR VOLUMES

meso-Aryl-Substituted [26]Hexaphyrin(1.1
meso-Aryl-Substituted [26]Hexaphyrin(1.1.0.1.1.0) and [38]Nonaphyrin(1.1.0.1.1.0.1.1.0) from Oxidative Coupling of a Tripyrrane
✍ Soji Shimizu; Ryuichiro Taniguchi; Atsuhiro Osuka 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 208 KB

CH 2 Cl 2 which contained 2 (107 mg, 24 %). The first eluted fraction from the alumina column was further purified by column chromatography on silica gel using a mixture of CH 2 Cl 2 /hexane as eluent to give a green fraction of 3 (38 mg, 8.5 %; see Table 1).

Dioxa-[40]decaphyrin(1.0.1.0.0.1.0.1.0.0
Dioxa-[40]decaphyrin(1.0.1.0.0.1.0.1.0.0): An analogue of turcasarin with a “figure-eight” structure
✍ Jonathan L. Sessler; Daniel Seidel; Andreas Gebauer; Vincent Lynch; Khalil A. Ab 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 122 KB

## Abstract The synthesis and characterization of two different furan containing analogues of turcasarin, namely 46,51 ‐dioxa‐2,11,15,20,24,33,37,42‐octapropyl‐turcasarin (**7a**) and 46,51 ‐dioxa‐2,11,24,33‐tetrapropyl‐15,20,37,42‐tetraethyl‐16,19,38,41‐tetramethyl‐turcasarin (**7b**) are describe