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Synthesis and structural study of [2.n](2,5)pyridinophanes

✍ Scribed by Takashi Funaki; Seiichi Inokuma; Hayato Ide; Tomomi Yonekura; Yosuke Nakamura; Jun Nishimura


Book ID
118501477
Publisher
Elsevier Science
Year
2004
Tongue
French
Weight
330 KB
Volume
45
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


Synthesis and structural studies of [n](
✍ Nobuhiro Kanomata; Makoto Nitta πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 French βš– 257 KB

The facile synthesis of [n](2,4)pyridinophane ring system (n = 9-6) was accomplished by the reaction of N-(1-phenylvinyl)iminophosphorane with cyclic ~1, H-unsaturated ketones. The chain flipping was studied by 'H NMR spectra at various temperatures.

Nicotinamide Coenzyme Models, I. Synthes
✍ Staab, Heinz A. ;Hasselbach, Hans-Joachim ;Krieger, Claus πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 790 KB

As nicotinamide coenzyme models the [2.2](2,5)pyridinophanes 3 -6 were prepared which consist of two interacting nicotinic ester units in the four different orientations possible. 3 -6 were obtained by photolytic sulfur extrusion from the corresponding dithia-[3.3](2,5)pyridinophanes 18-21 the synth