𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Preparation of Heptakis(2,6-di-O-ethyl)-β-cyclodextrin and Its Nuclear Magnetic Resonance Spectroscopic Characterization

✍ Scribed by Fumitoshi Hirayama; Masahiko Kurihara; Yasuhide Horiuchi; Tadanobu Utsuki; Kaneto Uekama; Masaki Yamasaki


Book ID
110379626
Publisher
Springer US
Year
1993
Tongue
English
Weight
838 KB
Volume
10
Category
Article
ISSN
0724-8741

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Stereoselective reduction of (R)-()-car
✍ Roberto Fornasier; Franco Marcuzzi; Michele Parmagnani; Umberto Tonellato 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 289 KB

Regio-and stereo-selective reduction of the double bonds in conjugated ketones with numerous reducing agents under various conditions have been studied'. The reactions usually afford mixtures of products, the compositions of which depend on the reagent, the catalyst, the solvent, the pH of the mediu

NMR spectroscopic properties of heptakis
✍ Wolfram Meier-Augenstein; Barend V. Burger; Hendrik S. C. Spies 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 413 KB

## Abstract The ^1^H and ^13^C NMR spectra of heptakis(2,6‐di‐__O__‐pentyl)‐β‐cyclodextrin in deuteriochloroform have been fully and unambiguously assigned. Several methods, including homo‐ and heteronuclear spin decoupling, two‐dimensional homo‐ and hetero‐nuclear correlation NMR spectroscopy, spe