1148136-35-9Relevant academic research and scientific papers
Total syntheses of (±)-taiwaniaquinol D and (±)-taiwaniaquinone D via a key Lewis acid-catalyzed Nazarov type cyclization
Kakde, Badrinath N.,Parida, Amarchand,Kumari, Pooja,Bisai, Alakesh
, p. 3179 - 3184 (2016/07/06)
Total syntheses of structurally intriguing taiwaniaquinoids viz (±)-taiwaniaquinol D (1e) and (±)-taiwaniaquinone D (1h) have been disclosed via a key Lewis acid catalyzed Nazarov type cyclization of arylvinylcarbinols.
A very efficient route toward the 4a-methyltetrahydrofluorene skeleton: short synthesis of (±)-dichroanone and (±)-taiwaniaquinone H
Alvarez-Manzaneda, Enrique,Chahboun, Rachid,Cabrera, Eduardo,Alvarez, Esteban,Alvarez-Manzaneda, Ramón,Meneses, Ricardo,Es-Samti, Hakima,Fernández, Antonio
supporting information; experimental part, p. 3384 - 3388 (2009/09/08)
A very expedient and efficient new route toward taiwaniaquinoids, bearing the 4a-methyltetrahydrofluorene skeleton, is reported. Key steps are the intramolecular Friedel - Crafts alkylation of an aryldiene and the degradative oxidation of a methylenedioxy
