Syntheses of spiroindole melatonin analogues via 2-(indolin-3-ylidene)acetonitrile cycloadditions

Autor:	S. E. Sosonyuk, Michael Yu. Seliverstov, Marina V. Proskurnina, V. V. Temnov, Nikolai S. Zefirov, Maria S. Volkova, N. A. Lozinskaya
Rok vydání:	2014
Předmět:	Melatonin chemistry.chemical_classification chemistry.chemical_compound Acetonitriles Double bond Chemistry medicine Organic chemistry General Chemistry Acetonitrile Cycloaddition medicine.drug
Zdroj:	Mendeleev Communications. 24:260-261
ISSN:	0959-9436
Popis:	2-(2-Oxo-1,2-dihydro-3H-indol-3-ylidene)acetonitriles were subjected to cycloaddition reactions at the double bond affording spiroindole melatonin analogues.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::61e8f11646b4c6d8b521c24f421636e4 https://doi.org/10.1016/j.mencom.2014.09.003 Zobrazit plný text záznamu Full Text from ScienceDirect