Highly diastereoselective synthesis of novel 2,3,4-trisubstituted chromanes via the reaction of 3-nitro-2-(trihalomethyl)- and 3-nitro-2-phenyl-2 H -chromenes with 1-morpholinocyclopentene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. A Condensation of Biginelli Products with 1,3‐Benzenediols: a Facile Access to Diastereomerically Pure Hexahydro‐5 H ‐chromeno[4,3‐ d ]pyrimidin‐5‐ones;ChemistrySelect;2019-08-30
2. Cesium-Carbonate-Mediated Benzalation of Substituted 2-Aryl-3-nitro-2H-chromenes with Substituted 4-Benzylidene-2-phenyloxazol-5(4H)-ones;Organic Letters;2019-04-02
3. Recent advances in the chemistry of 3-nitro-2H- and 3-nitro-4H-chromenes;Russian Chemical Reviews;2019-01-01
4. A regio- and stereocontrolled approach to the synthesis of 4-CF3-substituted spiro[chromeno[3,4-c]pyrrolidine-oxindoles]viareversible [3+2] cycloaddition of azomethine ylides generated from isatins and sarcosine to 3-nitro-2-(trifluoromethyl)-2H-chromenes;New Journal of Chemistry;2019
5. 3-Nitro-2-phenyl-2-(trifluoromethyl)-2H-chromenes in reaction with N-methylazomethine ylide: stereoselective synthesis of 3a,4,4-trisubstituted chromeno[3,4-c]pyrrolidines;Chemistry of Heterocyclic Compounds;2018-09
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