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Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2-a]carbazole Alkaloid Furoclausine-B | The Journal of Organic Chemistry
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![Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2-a]carbazole Alkaloid Furoclausine-B | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.8b02426/asset/images/medium/jo-2018-024266_0001.gif "Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2-a]carbazole Alkaloid Furoclausine-B | The Journal of Organic Chemistry")
Enantioselective Total Synthesis and Assignment of the Absolute Configuration of the Furo[3,2-a]carbazole Alkaloid Furoclausine-B | The Journal of Organic Chemistry
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Discovery of 4-(5-Methyloxazolo[4,5-b]pyridin-2-yl)-1,4-diazabicyclo[3.2.2]nonane (CP-810,123), a Novel α7 Nicotinic Acetylcholine Receptor Agonist for the Treatment of Cognitive Disorders in Schizophrenia: Synthesis, SAR Development, and in Vivo ...
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