Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small 
GTPase-targeting bicyclic peptides

Cromm, Philipp M.; Schaubach, Sebastian; Spiegel, Jochen; Fürstner, Alois; Grossmann, Tom; Waldmann, Herbert

doi:10.1038/ncomms11300

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Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides

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Cromm, Philipp M.
Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Spiegel, Jochen
Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Grossmann, Tom
Chemical Genomics Center of the MPS, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Waldmann, Herbert
Abt. IV: Chemische Biologie, Max Planck Institute of Molecular Physiology, Max Planck Society;

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Cromm, P. M., Schaubach, S., Spiegel, J., Fürstner, A., Grossmann, T., & Waldmann, H. (2016). Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides. Nature Communications, 7: 11300, pp. 1-7. doi:10.1038/ncomms11300.

Cite as: https://hdl.handle.net/11858/00-001M-0000-002A-3503-C

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