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Total Synthesis and Structural Revision of Cyclotetrapeptide Asperterrestide A

  • Kosuke Ohsawa
    Kosuke Ohsawa
    Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
  • Masato Sugai
    Masato Sugai
    Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
    More by Masato Sugai
  • Linnan Zhang
    Linnan Zhang
    Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
    More by Linnan Zhang
  • Yuichi Masuda
    Yuichi Masuda
    Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
  • Masahito Yoshida
    Masahito Yoshida
    Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
  • , and 
  • Takayuki Doi*
    Takayuki Doi
    Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aza-aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan
    *E-mail: [email protected]. Phone: +81-22-795-6865. Fax: +81-22-795-6864.
    More by Takayuki Doi
Cite this: J. Org. Chem. 2019, 84, 11, 6765–6779
Publication Date (Web):May 9, 2019
https://doi.org/10.1021/acs.joc.9b00526
Copyright © 2019 American Chemical Society
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Supporting Info (1)»

Abstract

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The structural revision of cyclotetrapeptide asperterrestide A has been achieved based on total synthesis and molecular modeling. For these studies, (2R,3S)-MePhe(3-OH) and (2S,3S)-MePhe(3-OH) suitably protected for peptide synthesis were prepared via a stereoselective reduction of a ketone precursor derived from L- or d-serine, using L-selectride or DIBAL-H. The synthesis of the proposed structure of asperterrestide A (1a) was accomplished by solution-phase synthesis of a linear precursor followed by macrolactamization. The NMR spectra of our synthetic 1a were not identical to those reported for the natural compound. Molecular modeling studies suggested that the correct structure 1b was the one in which the stereochemistry at the α-positions of the Ala and MePhe(3-OH) residues is the opposite to that of the proposed structure. This was confirmed by the total synthesis of 1b and its subsequent structural characterization.

Supporting Information

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The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.joc.9b00526.

  • 1H and 13C NMR for synthetic Fmoc-Ant-OH, 1a–b, 3, ent-3, 4a–b, 5a–b, 6a–b, 7a–b, 8a–b, 9a–b, 10, ent-10, 11a–b, 12, 13, 14, and 15, NOESY spectra for 1a–b, comparison of NMR spectroscopy data between natural 1 and synthetic 1a–b, conformers obtained by molecular mechanics calculation for 1d–f, correlation between observed NMR spectroscopy data and calculated values by molecular modeling, and biological assay data for 1a–b (PDF)

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Cited By


This article is cited by 3 publications.

  1. Shuang-Qi Tang, Maeva Leloire, Séverine Schneider, Julie Mohr, Jacques Bricard, Patrick Gizzi, Delphine Garnier, Martine Schmitt, Frédéric Bihel. Diastereoselective Synthesis of Nonplanar 3-Amino-1,2,4-oxadiazine Scaffold: Structure Revision of Alchornedine. The Journal of Organic Chemistry 2020, 85 (23) , 15347-15359. https://doi.org/10.1021/acs.joc.0c01764
  2. Kyriakos G. Varnava, Patrick J.B. Edwards, Alan J. Cameron, Elena Harjes, Vijayalekshmi Sarojini. Cyclic peptides bearing the d ‐Phe‐2‐Abz turn motif: Structural characterization and antimicrobial potential. Journal of Peptide Science 2021, 27 (2) https://doi.org/10.1002/psc.3291
  3. Anthony R. Carroll, Brent R. Copp, Rohan A. Davis, Robert A. Keyzers, Michèle R. Prinsep. Marine natural products. Natural Product Reports 2021, 37 https://doi.org/10.1039/D0NP00089B

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