✦ LIBER ✦

Acylation of a novel quinoxalinyl substituted pyrazole derivative. synthesis, quantum chemistry calculations, and x-ray structure analysis

✍ Scribed by Barbara Matuszczak; Thierry Langer; Kurt Mereiter

Publisher: Journal of Heterocyclic Chemistry
Year: 1998
Tongue: English
Weight: 240 KB
Volume: 35
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570350121

No coin nor oath required. For personal study only.

✦ Synopsis

The preparation of (N)-acetylpyrazolyl-quinoxalines and results of semiempirical MO calculations are presented. The structure determination of the isomers 3a,b was achieved by X-ray analysis.

📜 SIMILAR VOLUMES

ChemInform Abstract: Acylation of a Nove

ChemInform Abstract: Acylation of a Novel Quinoxalinyl Substituted Pyrazole Derivative. Synthesis, Quantum Chemistry Calculations, and X-Ray Structure Analysis.

✍ B. MATUSZCZAK; T. LANGER; K. MEREITER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Synthesis, Biological Activity, and X-Ra

Synthesis, Biological Activity, and X-Ray Crystal Structural Analysis of Diaryl Ether Inhibitors of Malarial Enoyl Acyl Carrier Protein Reductase. Part 1. 4′-Substituted Triclosan Derivatives.

✍ Joel S. Freundlich; et al. et al. 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 12 KB 👁 2 views

ChemInform Abstract: Synthesis, X-Ray Cr

ChemInform Abstract: Synthesis, X-Ray Crystal Structure, and Biological Activity of FR186054, a Novel, Potent, Orally Active Inhibitor of Acyl-CoA:Cholesterol O-Acyltransferase (ACAT) Bearing a Pyrazole Ring.

✍ A. TANAKA; T. TERASAWA; H. HAGIHARA; T. KINOSHITA; Y. SAKUMA; N. ISHIBE; M. SAWA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Synthesis and NMR investigation of 3,4-d

Synthesis and NMR investigation of 3,4-diazabicyclo[4.3.0]non-2-ene and N,N'-azo-3-azabicyclo[3.3.0]octane. X-ray crystal structure analysis of a new tetrazene derivative

✍ H. Delalu; M. Elkhatib; L. Peyrot; B. Fenet; B. F. Mentzen 📂 Article 📅 1999 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 433 KB

## Abstract 3,4‐Diazabicyclo[4.3.0]non‐2‐ene and __N,N'__‐azo‐3‐azabicyclo[3.3.0]octane are the main products of the oxidation of __N__‐amino‐3‐azabicyclo[3.3.0]octane by chloramine. These new compounds have been isolated and characterized. A structural study has been performed with the goal of est