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Model Synthetic Study of Tutin, a Picrotoxane-Type Sesquiterpene : Stereoselective Construction of a cis-Fused 5,6-Ring Skeleton

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/86538

Title: Model Synthetic Study of Tutin, a Picrotoxane-Type Sesquiterpene : Stereoselective Construction of a cis-Fused 5,6-Ring Skeleton
Authors: Ikeuchi, Kazutada Browse this author →KAKEN DB
Haraguchi, Shota Browse this author
Yamada, Hidetoshi Browse this author
Tanino, Keiji Browse this author →KAKEN DB
Keywords: picrotoxane-type sesquiterpene
desymmetrization
intramolecular aldol reaction
proline
Issue Date: 1-Jun-2022
Publisher: The Pharmaceutical Society of Japan (日本薬学会)
Journal Title: Chemical & pharmaceutical bulletin
Volume: 70
Issue: 6
Start Page: 435
End Page: 442
Publisher DOI: 10.1248/cpb.c22-00083
Abstract: Picrotoxinin, coriamyrtin, and tutin are representative natural products classified as picrotoxane-type sesquiterpenes and they function as strong neurotoxins. Because they possess a cis-fused 5,6-ring skeleton with a highly congested functionalization, organic chemistry researchers have pursued the development of a stereoselective synthesis method for such skeleton. This study aims to stereoselectively synthesize the cis-fused 5,6-ring skeleton with two tetrasubstituted carbons at both angular positions using a model compound. The results revealed that the desymmetrization of the 2-methyl-1,3-cyclopentanedione moiety via the DL-proline-mediated intramolecular aldol reaction of a pentanal derivative bearing an isopropenyl group and the (iv e-membered ring at the 3- and 5-position, respectively, provided the desired cis-fused skeleton. This reaction can construct four contiguous stereogenic centers of the bicyclic skeleton with the two angular positions in good yield with high stereoselectivity. Further, this reaction was applied to the kinetic resolution of the racemate using L-proline, providing the enantiomeric pure aldol product with the desired skeleton. This method can be utilized for total synthesis of picrotoxane-type sesquiterpenes.
Type: article
URI: http://hdl.handle.net/2115/86538
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 池内 和忠

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