Molecular iodine induced/1,3-dipolar cycloaddition/oxidative aromatization sequence: an efficient strategy to construct 2-substituted benzo[f]isoindole-1,3-dicarboxylates

Autor:	Jian-Rong Gao, Wu-Bin Yu, Huan-Ming Huang, Yu-Jin Li, Qing Ye, Wei-Jian Sheng
Rok vydání:	2014
Předmět:	Stereochemistry General Chemical Engineering Aromatization chemistry.chemical_element Sequence (biology) General Chemistry Oxidative phosphorylation Iodine Cycloaddition Quinone chemistry.chemical_compound chemistry 1 3-Dipolar cycloaddition Isoindole
Zdroj:	RSC Adv.. 4:15526-15533
ISSN:	2046-2069
DOI:	10.1039/c4ra01593b
Popis:	A useful method for a molecular iodine induced 1,3-dipolar cycloaddition/oxidative aromatization sequence to construct 2-substituted-benzo[f]isoindole-1,3-dicarboxylates is reported. This is the first report of a molecular iodine induced 1,3-dipolar cycloaddition between quinone structures and diethyl N-substituted iminodiacetates.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::49f1353b879a513b15d28e850fff0277 https://doi.org/10.1039/c4ra01593b Zobrazit plný text záznamu