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ORGANIC & BIOMOLECULAR CHEMISTRY
Volume -, Issue -, Pages -Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ob01580g
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A new thioxanthone-based photocatalyst with a [2.2]paracyclophane skeleton and planar chirality has been developed and successfully applied in visible light-mediated enantioselective reactions to produce azetidines. The structures of the catalyst derivatives were unequivocally determined by single crystal X-ray crystallography analysis.
A new thioxanthone-based photocatalyst with a [2.2]paracyclophane skeleton and planar chirality has been developed. The catalyst has been successfully applied in the visible light-mediated enantioselective aza Patern & ograve;-B & uuml;chi reactions of quinoxalinone and styrenes to produce azetidines. The structures of the catalyst derivatives were unequivocally determined by their single crystal X-ray crystallography analysis.
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