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Updated: Jan 27, 2026

In vitro Synthesis of Native, Fibrous Long Spacing and Segmental Long Spacing Collagen
Published on: September 20, 2012
Synthesis of the C21-C34 Segment of Aplyronine A toward Its Scalable Preparation
Madoka Suzuki1, Masahito Yoshida1,2,3, Hideo Kigoshi1,2,3,4
1Degree Programs in Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8571, Japan.
Abstract:
The development of scalable synthesis of the C21-C34 segment, a key intermediate for aplyronine A and its analogs, is reported. Marshall propargylation and Noyori asymmetric hydrogen transfer served as key reactions for the stereoselective construction of the desired C21-C34 segment on a gram scale. Further transformation of the segment successfully afforded the side chain analog that exhibited actin depolymerization activity similar to that previously reported.
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