Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: synthesis of trihalomethylated spiro[indoline-3,2′-pyrrolidin]-2-ones and spiro[indoline-3,3′-pyrrolizin]-2-ones › Research Explorer

Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: synthesis of trihalomethylated spiro[indoline-3,2′-pyrrolidin]-2-ones and spiro[indoline-3,3′-pyrrolizin]-2-ones

Research output: Contribution to journal › Article › peer-review

DOI

https://doi.org/10.1016/j.tet.2016.09.017
Final published version

Original language	English
Pages (from-to)	6825-6836
Number of pages	12
Journal	Tetrahedron
Volume	72
Issue number	43
DOIs	https://doi.org/10.1016/j.tet.2016.09.017
Publication status	Published - 27 Oct 2016

WoS ResearchAreas Categories

Chemistry, Organic

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Research areas

1,3-Dipolar cycloaddition, 3,3,3-Trihalogeno-1-nitropropenes, Spirooxindoles, Stabilised azomethine ylides

ID: 1180826