Construction of a pentacyclic ring system of isoryanodane diterpenoids by SmI2-mediated transannular cyclization |
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Authors: | Masaki Koshimizu Masanori Nagatomo Masayuki Inoue |
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Affiliation: | Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan |
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Abstract: | Isoryanodane diterpenoids possess a densely oxygenated and intricately fused pentacycle (ABCDE-ring), although its unique ring system has not yet been assembled chemically. The 6/5/7-membered BCD-rings of isoryanodanes differ from the 5/6/6-membered rings of the structurally-related ryanodanes. We previously achieved the total synthesis of ryanodine and five other ryanodane diterpenoids by employing the common ABDE-tetracyclic intermediate 1. Herein, we report a new strategy for constructing isoryanodane ABCDE-ring structure 3 from 1 via a combination of the oxy-Cope rearrangement and SmI2-mediated transannular cyclization. |
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Keywords: | Isoryanodane diterpenoids Natural product synthesis Oxy-Cope rearrangement Transannular cyclization Corresponding author. |
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