𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H and 13C NMR identification of unexpected 3,4-dihydroquinoxalines in the syntheses of 1,5-benzodiazepine derivatives

✍ Scribed by E. M. Tjiou; E. G. Lhoussaine; D. Virieux; A. Fruchier


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
141 KB
Volume
43
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The reaction between o‐phenylenediamines, dehydroacetic acid and aromatic aldehydes is shown to give not only the expected 1,5‐benzodiazepine derivative but also a 3,4‐dihydroquinoxaline, the structure of which was determined by its ^1^H and ^13^C 1D and 2D NMR spectra. Copyright © 2005 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Benzodiazepine analogues. Part 19.1H and
✍ Malose J. Mphahlele; Perry T. Kaye 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 103 KB 👁 1 views

Selected 1,4-and 1,5-benzoheterazepinones, prepared by the Schmidt rearrangement of flavanone analogues, were converted to the corresponding thiolactam derivatives using phosphorus pentasulfide. The proton and carbon chemical shifts of the thiolactam derivatives are compared with those of their lact

1H and 13C NMR spectral assignments of i
✍ Josefina Quirante; Faïza Diaba; Xavier Vila; Josep Bonjoch 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 79 KB

## Abstract The ^1^H and ^13^C NMR spectra of six 5‐substituted 2‐azabicyclo[2.2.2]octane derivatives were fully assigned by COSY and HSQC experiments. Copyright © 2005 John Wiley & Sons, Ltd.

NMR spectra and conformational analysis
✍ Farnaz Malik; Mashooda Hassan; Doris Rosenbaum; Helmut Duddeck 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 400 KB

An investigation of the molecular dynamics of substituted 1,3,4,5-tetrahydro-2H-l,Ibenzodiazepin-2-0ne derivatives revealed that these molecules adopt cycloheptadiene-like boat conformations. There is an equilibrium between the quasi-axial and the quasiequatorial conformer in which the quasi-axial c

IR, 1H NMR and 13C NMR spectra of isomer
✍ Pál Sohár; Ödön Fehér; Endre Tihanyi 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 371 KB

## Abstract The IR, ^1^H and ^13^C NMR spectra of six esters of 1‐aryl‐4‐methyl‐3‐ and 5‐pyrazolecarboxylic acids are reported. On the basis of their spectra the 3‐ or 5‐position of the substituent in such structural isomeric pairs can be established without recourse to the spectrum of the other me

1H and 13C NMR spectral characterization
✍ Xinxiang Lei; Lixue Zhang; Anjiang Zhang; Xiaoxia Ye; Jing Xiong 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 146 KB

## Abstract Some novel 1, 2, 4‐triazolo[3,4‐__b__][1,3,4]thiadiazines derivatives were synthesized. The complete ^1^H and ^13^C NMR chemical shift assignments were analyzed on one‐ and two‐dimensional NMR techniques, including DEPT, NOE‐DIF, COSY, HMBC, and HSQC. Copyright © 2006 John Wiley & Sons,