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Asymmetric synthesis of (+)-geranyllinaloisocyanide: assignment of absolute stereochemistry
Authors:Ichikawa Yoshiyasu  Matsuda Yasunori  Okumura Ken  Nakamura Mitsuhiro  Masuda Toshiya  Kotsuki Hiyoshizo  Nakano Keiji
Affiliation:Faculty of Science, Kochi University, Akebono-cho, Kochi, Japan. ichikawa@kochi-u.ac.jp
Abstract:The first nonracemic synthesis of (+)-geranyllinaloisocyanide, starting with (-)-lactic acid methyl ester, has been accomplished by exploiting a [3.3] sigmatropic rearrangement of allyl cyanate. The synthesis enables assignment of the S configuration of the C(3) isocyano substituted, quaternary stereogenic center in natural geranyllinaloisocyanide.
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