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Updated: Mar 7, 2026

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
Total Synthesis and Structural Revision of Clavilactone D
Ken-Ichi Takao1, Ryuichi Nemoto1, Kento Mori1
1Department of Applied Chemistry, Keio University, Hiyoshi, Kohoku-ku, Yokohama, 223-8522, Japan.
Abstract:
A structural revision of clavilactone D, a potent inhibitor of protein tyrosine kinases, was achieved by total syntheses of two newly proposed structures. The syntheses relied on ring-opening/ring-closing metathesis, which transformed a cyclobutenecarboxylate into a γ-butenolide. The syntheses confirmed that the correct structure of clavilactone D has an amino group at C-3 instead of a hydroxy group at C-2 in the originally proposed structure.
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