Highly diastereoselective 1,3-dipolar cycloaddition of nonstabilized azomethine ylides to 3-nitro-2-trihalomethyl-2H-chromenes: synthesis of 1-benzopyrano[3,4-c]pyrrolidines › Research Explorer

Highly diastereoselective 1,3-dipolar cycloaddition of nonstabilized azomethine ylides to 3-nitro-2-trihalomethyl-2H-chromenes: synthesis of 1-benzopyrano[3,4-c]pyrrolidines

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

DOI

https://doi.org/10.1016/j.tet.2013.07.080
Final published version

Original language	English
Pages (from-to)	8602-8608
Number of pages	7
Journal	Tetrahedron
Volume	69
Issue number	40
DOIs	https://doi.org/10.1016/j.tet.2013.07.080
Publication status	Published - 7 Oct 2013

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

WoS ResearchAreas Categories

Chemistry, Organic

Research areas

3-Nitro-2H-chromenes, Nonstabilized azomethine ylides, 1,3-Dipolar cycloaddition, 1-Benzopyrano[3,4-c]pyrrolidines, 3-NITROCHROMENE DERIVATIVES, STEREOSELECTIVE-SYNTHESIS, 3-SUBSTITUTED COUMARINS, RECEPTOR ANTAGONISTS, N-NUCLEOPHILES, C-NUCLEOPHILES, S-NUCLEOPHILES, 2-PI-COMPONENTS

ID: 858947