Synthesis of a Series of Novel Chiral Aromatic Heterocyclic Macrocycles Containing L-Amino Acid and 2,5-Bisphenyl-1,3,4-triazole Subunits

Autor:	Hong‐Wu Zhao, Wen-Ting Hua, Wei Yang, Rugang Zhong, Hong Yan, Jin Cui
Rok vydání:	2009
Předmět:	chemistry.chemical_classification chemistry.chemical_compound chemistry Yield (chemistry) Organic Chemistry Triazole Organic chemistry Enantiomer Condensation reaction Combinatorial chemistry Chiral diamine Amino acid Dichloromethane
Zdroj:	Synthetic Communications. 39:3038-3044
ISSN:	1532-2432 0039-7911
DOI:	10.1080/00397910902730879
Popis:	An array of novel chiral aromatic heterocyclic macrocycles, which may show potential enantiomeric recognition to variable D- and L-amino acids, were synthesized in acceptable yield. The desired macrocycles 3a–c and 4a–c were obtained via the condensation reaction of chiral diamine intermediates 2a–c with 2,5-bis(o-chloroformylphenyl)-1,3,4-triazole 5 in a presence of Et3N in a highly diluted dichloromethane solution at room temperature.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::8fb42800c11263844cee4d3b378b2a54 https://doi.org/10.1080/00397910902730879 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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