𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Configuration and conformational mobility of [12] annulene from NMR studies at various temperatures

✍ Scribed by Jean F.M. Oth; J.-M. Gilles; G. Schröder


Publisher
Elsevier Science
Year
1970
Tongue
French
Weight
315 KB
Volume
11
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


As shown in the preceding note 2) , a 75% pure [ lZ]annulene can be synthesized by UV irradiation of syn-tricyclo[ 8.2.0.0 2'9]d d o eta-3.5.7.1i-tetraene at -ilO"C. We have investigated the temperature dependent NMR spectrum of this compound in order i) to establish its configuration in terms of the number and the sequence of cis and trans double bonds, and ii) to study the reversible dynamic process occurring in this molecule.


📜 SIMILAR VOLUMES


Configurational and conformational study
✍ M. J. Fernández; R. Huertas; M. S. Toledano; E. Gálvez; J. Server; M. Martínez-R 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 342 KB 👁 2 views

A series of esters derived from synand anti-2-methyl-2-azabicyclo [ 2.2.2 ] octan-5-ols were synthesized and studied by 1H, 13C and 2D NMR spectroscopy. The crystal structure of 5-syn-(3,5-dichlorobenzoyloxy)-2-methyl-2azabicyclo [ 2.2.2 ] octane was determined by x-ray di †raction. The unambiguous

Conformational Studies of Marine Polyhal
✍ Graziano Guella; Giuseppe Chiasera; Francesco Pietra 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 German ⚖ 911 KB

~e~~~ a-Chamigren-3-one (+)-8 bearing an axial C1-atom at C(8) exists as a largely dominant conformer with MeeC(5) at the envelope-shaped enone ring pointing away from CI,,-C(8) at the cyclohexane ring ( = B) in the 'normal' chair conformation, as shown by 'H-NMR. In contrast, the a -chamigren-3-ols

Conformational Studies of Marine Polyhal
✍ Graziano Guella; Giuseppe Chiasera; Francesco Pietra 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 German ⚖ 779 KB

## 3. VII. 92) Temperature-dependent NMR spectra indicate that the a -chamigren-3-ones (-)-11, (+)-12, (+)-14 (-)-15, (+)-16,18, and 19 bearing equatorial halogen atoms at C(8) and C(9) undergo slow conformational flipping of the envelope-shaped enone ring, while the cyclohexane ring is maintained