✦ LIBER ✦

Preparation of some dibenz[b,f][1,4]oxazepines and dibenz[b,e]azepines

✍ Scribed by Wardrop, Arthur W. H.; Sainsbury, Gordon L.; Harrison, John M.; Inch, Thomas D.

Book ID: 115505564
Publisher: Royal Society of Chemistry
Year: 1976
Weight: 865 KB
Volume: 12
Category: Article
ISSN: 1472-7781
DOI: 10.1039/p19760001279

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: 11H-Dibenz[b,e]azep

ChemInform Abstract: 11H-Dibenz[b,e]azepines. Part 1. Synthesis and IR Spectra of Dibenz[b,f][1,4]oxazepines.

✍ V. G. NOSKOV; L. N. KALININA; M. N. NOSKOVA; YU. L. KRUGLYAK; O. G. STRUKOV; A. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

ChemInform Abstract: 11H-Dibenz[b,e]azep

ChemInform Abstract: 11H-Dibenz[b,e]azepines. Part 2. Synthesis of 10-15N-Dibenz[b,f][1,4]oxazepine (II).

✍ V. G. NOSKOV; YU. L. KRUGLYAK; O. G. STRUKOV; V. K. KUROCHKIN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Neue Synthese von Lactamen der Dibenz[b,

Neue Synthese von Lactamen der Dibenz[b,f]-1,4-thiazepin-, -oxazepin und Dibenz[b, e]-azepin-Reihe. 4. Mitteilung über siebengliedrige Heterocyclen

✍ J. Schmutz; F. Künzle; F. Hunziker; A. Bürki 📂 Article 📅 1965 🏛 John Wiley and Sons 🌐 German ⚖ 680 KB

11H-dibenz[b,e]azepines. Part 4. Protona

11H-dibenz[b,e]azepines. Part 4. Protonated and N-alkylated compounds of dibenz[b,f]-1,4-ox(thia)azepine

✍ V. G. Noskov; L. N. Kalinina; M. N. Noskova; Yu. L. Kruglyak; O. G. Strukov; V. 📂 Article 📅 1998 🏛 Springer 🌐 English ⚖ 217 KB

Oxidation of some dibenz[b,f][1,4]oxazep

Oxidation of some dibenz[b,f][1,4]oxazepines by peracetic acid

✍ Brewster, Keith; Chittenden, Rosemary A.; Harrison, John M.; Inch, Thomas D.; Br 📂 Article 📅 1976 🏛 Royal Society of Chemistry ⚖ 678 KB

Dibenz[b,f]azepines, Part 7[1]: Synthesi

Dibenz[b,f]azepines, Part 7[1]: Synthesis of New, Potentially CNS Active Dibenz[b,f]azepine Derivatives

✍ Ferenc Haász; Zoltán Tóth; Vilmos Galamb 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 315 KB 👁 1 views

Reactions of 5-carboxamido-5H-dibenz[bflazepines (la-ld) with glyoxylic acid methylester methyl hemiacetal (GMHA) led to 5-(carboxamido-N-a-hydroxy-acetic acid methyl ester)-5Hdibenz[b,Aazepines (2a-2d). The reactions with glycols yielded the oligoethylene glycol derivatives (3,4). The new compounds