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Alternative General Synthetic Routes to [2.2]Cyclophanes and [3.2]Cyclophanes from [3.3]Cyclophane-2,11-diones by Photodecarbonylation, and a Structural Study of [3.2]Metacyclophanes

✍ Scribed by Hajime Isaji; Mikio Yasutake; Hiroyuki Takemura; Katsuya Sako; Hitoshi Tatemitsu; Takahiko Inazu; Teruo Shinmyozu


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
748 KB
Volume
2001
Category
Article
ISSN
1434-193X

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📜 SIMILAR VOLUMES


Cyclophanes, XXXV. DNMR, molecular mecha
✍ Bodwell, Graham J. ;Ernst, Ludger ;Hopf, Henning ;Jones, Peter G. ;McNally, John 📂 Article 📅 1990 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 515 KB

## Abstract The syntheses of 2,11‐dithia[3,3]orthometacyclophane (5) and 2,11‐dithia[3,3]orthoparacyclophane (6) by dithiol‐dibromide coupling are described. Whereas the yield of 5 is not significantly affected by the substrate pairing, that of 6 is. Both compounds exhibit a temperature‐dependent ^

Solid-State Structural Study of the Char
✍ Mikio Yasutake; Koji Araki; Ming Zhou; Rika Nogita; Teruo Shinmyozu 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 277 KB 👁 1 views

## Abstract 5,7,9‐Trimethyl[3~3~](1,3,5)cyclophane (1), with two binding sites of different donating ability, adopts a __C__~3~ conformation both in the solid state (−170 °C) and in CD~2~Cl~2~ solution at −90 °C. 5,7,9‐Trimethyl[3~3~](1,3,5)cyclophane‐2,11,20‐trione (9) has the same __C__~3~ symmet