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Synthesis of (-)-agelastatin A by [3.3] sigmatropic rearrangement of allyl cyanate
Authors:Ichikawa Yoshiyasu  Yamaoka Tomonori  Nakano Keiji  Kotsuki Hiyoshizo
Affiliation:Faculty of Science, Kochi University, Kochi 780-8520, Japan. ichikawa@kochi-u.ac.jp
Abstract:Total synthesis of (-)-agelastatin A has been achieved starting from l-arabitol. The highlights in our synthesis include the preparation of vicinal diamine moiety by [3.3] sigmatropic rearrangement of allyl cyanate and construction of central ring-C with ring-closing metathesis.
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