Synthesis of optically active 6-substituted 2-(aminomethyl)chromans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Synthesis of ethyl 6-substituted-chroman- and -chromone-2-carboxylates. Comparative structure-activity study employing the 6-phenyl and phenoxy analogs in the triton hyperlipidemic rat model
2. A Potent Aldose Reductase Inhibitor, (2S,4S)-6-Fluoro-2‘,5‘-dioxospiro[chroman-4,4‘-imidazolidine]-2-carboxamide (Fidarestat): Its Absolute Configuration and Interactions with the Aldose Reductase by X-ray Crystallography
3. N-[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines: Synthesis and Wide Range of Antagonism at the Human 5-HT1A Receptor
4. Novel derivatives of 3-(dipropylamino)chroman. Interactions with 5-HT1A and D2A receptors
5. 2-(Aminomethyl)chromans that inhibit iron-dependent lipid peroxidation and protect against central nervous system trauma and ischemia
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4. Sulfoxide-Directed Stereocontrolled Access to 2H-Chromans: Total Synthesis of the (S,R,R,R)-Enantiomer of the Antihypertensive Drug Nebivolol;European Journal of Organic Chemistry;2008-04
5. A highly efficient enantioselective synthesis of 2-methyl chromans via four sequential palladium-catalyzed reactions;Tetrahedron Letters;2005-02
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