✦ LIBER ✦

Heteroadamantanes and their derivatives. 7. Synthesis and mass-spectrometric study of functional derivatives of 5-mono- and 5,7-disubstituted 1,3-diazaadamantanes

✍ Scribed by A. I. Kuznetsov; E. B. Basargin; M. Kh. Ba; A. S. Moskovkin; I. V. Miroshnichenko; M. Ya. Botnikov

Publisher: Springer US
Year: 1989
Tongue: English
Weight: 542 KB
Volume: 25
Category: Article
ISSN: 0009-3122
DOI: 10.1007/bf00482502

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Heteroadamantanes and their derivatives.

Heteroadamantanes and their derivatives. 9. Synthesis of 1,5-dinitro-3,7-diazabicyclo[3.3.1]nonane and derived 2,2-disubstituted 5,7-dinitro-1,3-diazaadamantanes

✍ A. I. Kuznetsov; K. I. Romanova; E. B. Basargin; A. S. Moskovskii; B. V. Unkovsk 📂 Article 📅 1990 🏛 Springer US 🌐 English ⚖ 339 KB

Heteroadamantanes and their derivatives.

Heteroadamantanes and their derivatives. 10. Hydrolysis of 7-bromo-1,3,5-triazaadamantane

✍ A. I. Kuznetsov; V. A. Tyurikov; V. A. Kosmakov 📂 Article 📅 1990 🏛 Springer US 🌐 English ⚖ 235 KB

Synthesis of 6-Mono- and 5,6-Disubstitut

Synthesis of 6-Mono- and 5,6-Disubstituted 1,2,3-Triazolo[4,5-d]pyrimidin-7-ones.

✍ V. P. Kislyi; E. B. Danilova; V. V. Semenov 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 102 KB 👁 1 views

Synthesis, Lipophilicity and Structure o

Synthesis, Lipophilicity and Structure of 2,5-Disubstituted 1,3,5-Dithiazine Derivatives.

✍ Leyte Winfield; Chunming Zhang; Christy A. Reid; Edwin D. Stevens; Mark L. Trude 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 95 KB 👁 1 views

Synthesis, lipophilicity and structure o

Synthesis, lipophilicity and structure of 2,5-disubstituted 1, 3, 5-dithiazine derivatives

✍ Leyte Winfield; Chunming Zhang; Christy A. Reid; Edwin D. Stevens; Mark L. Trude 📂 Article 📅 2003 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 72 KB

## Abstract A series of 2,5‐disubstituted 1,3,5‐dithiazine derivatives were synthesized as potential analogues of the potent dopamine uptake inhibitor GBR 12909. The lipophilic character of the 1,3,5‐dithiazine derivatives were experimentally (log __P__) and computationally (clog __P__) determined.

Density functional study of tricyclo[3,3

Density functional study of tricyclo[3,3,1,13,7]decane and tricyclo[3,3,1,13,7]decsilane and their halogen derivatives

✍ Li-Hwa Lu 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 186 KB

10 12 4 10 12 4 Ionization potentials, HOMO and LUMO energies, energy gaps, heats of formation, atomization energies, and vibration frequencies were calculated. These calculations w 3,7 x indicate that these molecules are stable and have T symmetry. Tricyclo 3,3,1,1 decd Ž . silane and its halogen