1-Acyldihydropyridones as Synthetic Intermediates
The most efficient and stereoselective total synthesis of (+/-) lausbine II to date has been achieved. The key steps in this are the copper-mediated conjugate addition reaction of the Grignard reagent of 1-bromo-4-chlorobutane to a dihydropyridone and a stereoselective reduction of a quinolizidinone...
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| Format: | Others |
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DigitalCommons@USU
1988
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| Online Access: | https://digitalcommons.usu.edu/etd/7180 https://digitalcommons.usu.edu/cgi/viewcontent.cgi?article=8288&context=etd |