## Abstract Chemical shifts are reported for the heterocyclic ring hydrogen of a series of __para__‐substituted 4‐aryl‐1,2,3‐selenadiazoles and substituent effects are evaluated statistically by means of the Swain‐Lupton multiple correlation analysis. A satisfactory understanding of the various sub
New many fold 1,2,3-selenadiazole aromatic derivatives
✍ Scribed by Mousa Al-Smadi; Samer Ratrout
- Book ID
- 102342928
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2004
- Tongue
- English
- Weight
- 56 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The many fold aromatic ketones 2a‐d are versatile compounds for the synthesis of the many fold 1,2,3‐selenadiazole aromatic derivatives 5a‐d. The preparation starts with the reaction between the many fold bromomethylene benzene derivatives 1a‐d and 4‐hydroxyacetophenone, which are transformed through the reaction with semicarbazide hydrochloride or ethylhydrazine carboxylate into the corresponding semicarbazones derivatives 3a‐d or hydrazones 4a‐d. The reaction with selenium dioxide leads to regiospecific ring closure of semicarbazones or hydrazones to give the many fold 1,2,3‐selenadiazole aromatic derivatives in high yield.
📜 SIMILAR VOLUMES
## Abstract Durch Addition von Acylhydrazinen an Aryl‐ oder Alkyl‐ bzw. Acyl‐isoselenocyanate werden in guten Ausbeuten 1,4‐disubstituierte Selenosemicarbazide gebildet. Die aus Selenosenfölen mit 4‐Aryl‐selenosemicarbaziden primär erhältlichen Hydrazin‐N, N′‐bis‐selenocarbonsäureamide cyclisieren
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract Novel sulfur‐linked bis‐heterocycles, bis‐1,2,3‐selenadiazoles **4**, 1,2,3‐thiadiazoles **5**, and 2__H__‐diazaphospholes **7**, were synthesized from bis(2‐oxo‐2‐phenylethanone)sulfide **2** by adopting a simple and well‐versed methodology. © 2008 Wiley Periodicals, Inc. Heteroatom Ch