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Study of 1,3-dipolar cycloaddition of amino-acid azomethines and Juglone.
- Source :
-
Synthetic Communications . 2020, Vol. 50 Issue 20, p3165-3173. 9p. 7 Diagrams. - Publication Year :
- 2020
-
Abstract
- Novel 2,3,4,9-tetrahydro- and 4,9-dihydro-1H-benzofisoindole derivatives were synthesized from Juglone and amino-acid azomethines in 74–85% yields via 1,3-dipolar cycloaddition. The stereo- and regioselectivity of cycloaddition was confirmed by NMR spectra and single-crystal X-ray diffraction analysis. [ABSTRACT FROM AUTHOR]
- Subjects :
- *RING formation (Chemistry)
*ISOXAZOLIDINES
*X-ray spectra
*X-ray diffraction
Subjects
Details
- Language :
- English
- ISSN :
- 00397911
- Volume :
- 50
- Issue :
- 20
- Database :
- Academic Search Index
- Journal :
- Synthetic Communications
- Publication Type :
- Academic Journal
- Accession number :
- 146465889
- Full Text :
- https://doi.org/10.1080/00397911.2020.1795880