Synthesis of bis-spirofused thiapyrrolizidinooxindoles by 1,3-dipolar cycloaddition

Autor:	Yu. V. Nelyubina, Konstantin A. Lyssenko, A. A. Shvets, Sergey V. Kurbatov
Rok vydání:	2012
Předmět:	chemistry.chemical_compound Addition reaction Rhodanine chemistry Isatin 1 3-Dipolar cycloaddition Thiaproline Azomethine ylide Organic chemistry General Chemistry Cycloaddition
Zdroj:	Russian Chemical Bulletin. 61:1659-1662
ISSN:	1573-9171 1066-5285
DOI:	10.1007/s11172-012-0227-y
Popis:	The 1,3-dipolar cycloaddition of unstabilized azomethine ylide, which is generated in situ from isatin and thiaproline, to arylidene derivatives of rhodanine affords bis-spirofused thiapyrrolizidinooxindoles. The 1,3-dipolar addition reactions under consideration are fully regio- and diastereoselective.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::0bc5767c66b33d437fd9affa15410e0c https://doi.org/10.1007/s11172-012-0227-y Zobrazit plný text záznamu Full text from SpringerLink