𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Formation of 1H-2,3-dihydro-2,2,4-trimethyl-1,5-benzodiazepine from o-phenylenediamine and acetone

✍ Scribed by A. N. Kost; Z. F. Solomko; L. N. Polovina; L. G. Gergel


Book ID
112326313
Publisher
Springer US
Year
1971
Tongue
English
Weight
212 KB
Volume
7
Category
Article
ISSN
0009-3122

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of 2,5,8-trimethyl-3,4-dihydro
✍ E. J. Eisenbraun; B. Dewprashad; P. W. Geno; A. R. Taylor 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 168 KB

## Abstract The synthesis of specifically labeled 2,5,8‐trimethyl‐3,4‐dihydro‐1(2H)‐naphthalenone‐2‐d and 3,5,8‐trimethyl‐3,4‐dihydro‐1(2H)‐naphthalenone‐2,2‐d~2~ through α‐proton exchange using neat trifluoroacetic acid‐d is described.

2,4-Bis(4-chlorophenyl)-2-methyl-2,3-dih
✍ An, Li-Tao ;Ding, Fei-Qing ;Zou, Jian-Ping ;Lu, Xiao-Hua 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 989 KB

In the title compound, C 22 H 18 C l2 N 2 , the seven-membered heterocyclic ring is in a boat-shaped conformation. The molecules are linked by N-HÁ Á ÁN hydrogen bonding into one-dimensional chains along the [010] direction.