BIOMIMETIC SYNTHESIS OF NAUCLEA INDOLE ALKALOIDS, NAUCLEIDINAL, AND 3-EPI-NAUCLEIDINAL, BY STEREOSELECTIVE REARRANGEMENT OF STRICTOSAMIDE AND THE VINCOSIDE LACTAM AGLYCONES
著者所属:Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University
Based on a biogenetic consideration, a Nauclea alkaloid, naucleidinal (6), and its 3-epimer (7) were stereoselectively prepared from the aglycones of strictosamide and the vincoside lactam, and their absolute stereochemistry was confirmed.