Highly stereoselective [3+2]-cycloaddition reaction of stabilised N,N′-cyclic azomethine imines with 3-nitro-2-phenyl-2H-chromenes: Synthesis of tetrahydrochromeno[4,3-c]pyrazolo[1,2-a]pyrazol-11-ones › Research Explorer

Highly stereoselective [3+2]-cycloaddition reaction of stabilised N,N′-cyclic azomethine imines with 3-nitro-2-phenyl-2H-chromenes: Synthesis of tetrahydrochromeno[4,3-c]pyrazolo[1,2-a]pyrazol-11-ones

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

DOI

https://doi.org/10.1016/j.tetlet.2017.09.015
Final published version

Original language	English
Pages (from-to)	3989-3992
Number of pages	4
Journal	Tetrahedron Letters
Volume	58
Issue number	42
DOIs	https://doi.org/10.1016/j.tetlet.2017.09.015
Publication status	Published - 18 Oct 2017

WoS ResearchAreas Categories

Chemistry, Organic

Research areas

1,3-Dipolar cycloaddition, 2-Arylmethylidene-5-oxopyrazolidin-2-ium-1-ides, 3-Nitro-2-phenyl-2H-chromenes, Tetrahydrochromeno[4,3-c]pyrazolo[1,2-a]pyrazol-11-ones

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

ID: 2124069