Total synthesis of the antifungal depsipeptide petriellin A

Date

2011

Authors

Sleebs, M.
Scanlon, D.
Karas, J.
Maharani, R.
Hughes, A.

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Journal article

Citation

Journal of Organic Chemistry, 2011; 76(16):6686-6693

Statement of Responsibility

Marianne M. Sleebs, Denis Scanlon, John Karas, Rani Maharani, and Andrew B. Hughes

Conference Name

Abstract

We report the solid-phase total synthesis of the antifungal highly modified cyclic depsipeptide petriellin A. The synthesis confirms earlier reports on the absolute configuration of the natural product. The solid-phase approach resulted in a protected linear precursor, which was cleaved from the solid support prior to cyclization and final deprotection. Use of advanced coupling agents for several hindered amides was a feature of the synthesis. The natural product was prepared in overall 5% yield.

School/Discipline

School of Chemistry and Physics

Dissertation Note

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Description

Publication Date (Web): July 8, 2011

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Rights

© 2011 American Chemical Society

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