Resynthesis of phalloidin and phallisin from the seco‐compounds

Munekata, Eisuke; Faulstich, Heinz; Wieland, Theodor

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Resynthesis of phalloidin and phallisin from the seco‐compounds

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Munekata, Eisuke
Max Planck Institute for Medical Research, Max Planck Society;

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Faulstich, Heinz
Department of Molecular Cell Research, Max Planck Institute for Medical Research, Max Planck Society;

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Wieland, Theodor
Max Planck Institute for Medical Research, Max Planck Society;

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https://onlinelibrary.wiley.com/doi/epdf/10.1002/anie.197702671
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https://doi.org/10.1002/anie.197702671
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Citation

Munekata, E., Faulstich, H., & Wieland, T. (1977). Resynthesis of phalloidin and phallisin from the seco‐compounds. Angewandte Chemie International Edition in English, 16(4), 267-268.

Cite as: https://hdl.handle.net/21.11116/0000-0002-CCE2-9

Abstract

The cyclic peptides (1) from the green deathcup toadstool can be cleaved specifically (arrow). Ring closure of the seco‐compounds obtained in highly pure form has now been accomplished. Thus the total synthesis and synthesis of analogs have become a step nearer.
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