Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Organic Chemistry Regular Papers
Synthesis of (+)-Aptosimon, a 4-Oxofurofuran Lignan, by erythro Selective Aldol Condensation and Stereoconvergent Cyclization as the Key Reactions
Satoshi YAMAUCHIMunetoshi YAMAGUCHI
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2003 Volume 67 Issue 4 Pages 838-846

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Abstract
   The 4-oxofurofuran lignan, (+)-aptosimon (1), was synthesized from γ-butyrolactone (9). To construct the two benzylic chiral center of (+)-aptosimon (1), highly erythro selective aldol condensation and stereoconvergent SN1 intramolecular cyclization were used as the key reactions.
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© 2003 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
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