## Abstract The ^1^H and ^13^C NMR spectra of 4,8,9,10‐tetraaryl‐1,3‐diazatricyclo[3.3.1.13, 7]decan‐6‐ones were measured at 400 and 500 and at 100 and 125 MHz, respectively. The chemical shifts were assigned unambiguously using one‐ and two‐dimensional (H,H‐COSY, C,H‐COSY, NOESY, ROESY and HMBC) N
✦ LIBER ✦
Synthesis and characterization of 9,10-diethyl-2,4,6,8-tetraoxa-1,3,5,7-tetraarsatricyclo[3.3.1.13,7]decane (I) and S-9,10-dimethyl-2,4,6,8-tetraoxa-1,3,5,7-tetraarsatricyclo[3.3.1.13,7]decane (II), two compounds analogous to As(III)oxide
✍ Scribed by M.B.L. Marx; H. Pritzkow; B.K. Keppler
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 57 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0162-0134
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A 1H and 13C NMR study of 4,8,9,10-tetra
✍
V. Vijayakumar; M. Sundaravadivelu; S. Perumal; A. Lycka
📂
Article
📅
2001
🏛
John Wiley and Sons
🌐
English
⚖ 85 KB
ChemInform Abstract: Regioselective Synt
✍
Glen P. Miller; Ingyu Jeon; A. Nikki Faix; Jerry P. Jasinski; Andreas J. Athans;
📂
Article
📅
2000
🏛
John Wiley and Sons
⚖ 39 KB
👁 2 views
Synthesis and X-Ray Structural Studies o
✍
Przemyslaw Gluziński; Janusz Jurczak; Janusz W. Krajewski; Piotr Sałański; Tomas
📂
Article
📅
1992
🏛
John Wiley and Sons
🌐
German
⚖ 306 KB
👁 1 views
## Abstract The molecular structures of the title compounds 3 and 5 were investigated by NMR and X‐ray structural methods. The NMR results suggest two equivalent halves for both molecules. The X‐ray study shows an approximate mirror plane for 3 and an approximate twofold axis for a significant port
Synthesis and Rotamerism of 9,10-Diaryl-
✍
V. A. Chebanov; V. E. Saraev; K. M. Kobzar; S. M. Desenko; V. D. Orlov; E. A. Gu
📂
Article
📅
2004
🏛
John Wiley and Sons
⚖ 16 KB
👁 1 views
ChemInform Abstract: Synthesis and Cryst
✍
B. KOKEL; B. BACHET; A. COUSSON
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 27 KB
👁 2 views
Synthesis of bridged analogs of epibatid
✍
Lawrence E Brieaddy; S Wayne Mascarella; Hernán A Navarro; Robert N Atkinson; M.
📂
Article
📅
2001
🏛
Elsevier Science
🌐
French
⚖ 86 KB
The synthesis of conformationally locked analogs of epibatidine are described in which the key step is an intramolecular reductive palladium-catalyzed Heck-type coupling.