Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers

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

Original language	English
Pages (from-to)	531-540
Number of pages	10
Journal	Chemistry of Heterocyclic Compounds
Volume	51
Issue number	6
DOIs	https://doi.org/10.1007/s10593-015-1733-2
Publication status	Published - Jun 2015

chromans, 3-nitro-2H-chromenes, push-pull enamines, atropisomerism, nucleophilic addition, POTASSIUM CHANNEL ACTIVATORS, ANTIHYPERTENSIVE ACTIVITY, STEREOSELECTIVE ADDITION, MICHAEL ADDITION, N-NUCLEOPHILES, C-NUCLEOPHILES, S-NUCLEOPHILES, 3-NITRO-2-TRIHALOMETHYL-2H-CHROMENES, 3-NITRO-2H-CHROMENES, ISOMERS

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