Syntheses of 6-Amino-1,3-benzodioxin and Its p-Arylazo-Substituted Calix[4]arenes

Autor:	Mei-Ling Yeh, Wen-Chin Liu, Fa-Shin Tang, Lee-Gin Lin, Shu-Ling Chen
Rok vydání:	1994
Předmět:	chemistry.chemical_classification Azo compound Diazonium Compounds Bicyclic molecule Organic Chemistry chemistry.chemical_element Medicinal chemistry Coupling reaction chemistry.chemical_compound chemistry Calixarene Organic chemistry Diazo Palladium Cyclophane
Zdroj:	The Journal of Organic Chemistry. 59:754-757
ISSN:	1520-6904 0022-3263
DOI:	10.1021/jo00083a015
Popis:	The p-arylazo-substituted calix[4]arenes were synthesized by a diazo- coupling reaction between calix[4]arene and the diazonium salt of 6-amino-1,3-benzodioxin. The monoarylazo-, 1,2-diarylazo-, 1,3-diaryl- azo- , triarylazo-, and tetraarylazo-para-substituted calix[4]arenes were isolated and characterized by spectral methods. 6-Amino-1,3-benzo- dioxin was prepared by palladium metal reduction of 6-nitro-1,3-benzo- dioxin
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::6df4ae7c277d3bd17491d476c79c944f https://doi.org/10.1021/jo00083a015 Zobrazit plný text záznamu