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3-Cyanochromones in [3+2] cycloadditions with an azomethine ylide derived from sarcosine and formaldehyde. A short synthesis of 1-benzopyrano[2,3-c:3,4- c′]dipyrrolidines
Research output
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Contribution to journal
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Article
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peer-review
Department of Organic Chemistry
Section of Chemical Material Science
Institute of Natural Sciences and Mathematics
Overview
Cite this
DOI
https://doi.org/10.1016/j.tetlet.2013.10.154
Final published version
Vyacheslav Ya. Sosnovskikh
Mikhail Yu. Kornev
Vladimir S. Moshkin
Original language
English
Pages (from-to)
212-214
Number of pages
3
Journal
Tetrahedron Letters
Volume
55
Issue number
1
DOIs
https://doi.org/10.1016/j.tetlet.2013.10.154
Publication status
Published -
1 Jan 2014
ASJC Scopus subject areas
Organic Chemistry
Drug Discovery
Biochemistry
Research areas
3-Cyanochromones, Nonstabilized azomethine ylide, [3+2] Cycloaddition, 1-Benzopyrano[2,3-c]pyrrolidines, Recyclization, Hexahydrochromeno[2,3-c:3,4-c ']dipyrroles, ALPHA-AMINO-ACIDS, 1,3-DIPOLAR CYCLOADDITIONS, DECARBOXYLATIVE TRANSAMINATION, 3-NITROCHROMENE DERIVATIVES, 3-SUBSTITUTED COUMARINS, MECHANISM, ROUTE, 2-PI-COMPONENTS
ID: 291909