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Applying Mosher's method to acetogenins bearing vicinal diols. The absolute configurations of muricatetrocin C and rollidecins A and B, new bioactive acetogenins from Rollinia mucosa

✍ Scribed by Guoen Shi; Zhe-ming Gu; Kan He; Karl V. Wood; Lu Zeng; Qing Ye; John M. MacDougal; Jerry L. McLaughlin


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
588 KB
Volume
4
Category
Article
ISSN
0968-0896

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✦ Synopsis


Muricatetrocin C (l), rollidecin A (2), and rollidecin B (3), three new bioactive annonaceous acetogenins bearing vicinal diols, were isolated from the leaves of Rollinia mucosa (Annonaceae) using activity-directed fractionation. The total structural elucidations of 1-3, including the absolute stereochemistries of the vicinal diols, were achieved by analyzing their per-Mosher ester derivatives. All three compounds showed potent and selective inhibitory effects against several human cancer cell lines.