Modular terpene synthesis enabled by mild electrochemical couplings

Author:

Harwood Stephen J.1ORCID,Palkowitz Maximilian D.1ORCID,Gannett Cara N.2ORCID,Perez Paulo3ORCID,Yao Zhen4ORCID,Sun Lijie4ORCID,Abruña Héctor D.2ORCID,Anderson Scott L.3ORCID,Baran Phil S.1ORCID

Affiliation:

1. Department of Chemistry, Scripps Research, La Jolla, CA 92037, USA.

2. Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853, USA.

3. Department of Chemistry, University of Utah, Salt Lake City, UT 84112, USA.

4. Asymchem Life Sciences (Tianjin) Co., Ltd., TEDA Tianjin, 300457, P.R. China.

Abstract

The synthesis of terpenes is a large field of research that is woven deeply into the history of chemistry. Terpene biosynthesis is a case study of how the logic of a modular design can lead to diverse structures with unparalleled efficiency. This work leverages modern nickel-catalyzed electrochemical sp 2 –sp 3 decarboxylative coupling reactions, enabled by silver nanoparticle–modified electrodes, to intuitively assemble terpene natural products and complex polyenes by using simple modular building blocks. The step change in efficiency of this approach is exemplified through the scalable preparation of 13 complex terpenes, which minimized protecting group manipulations, functional group interconversions, and redox fluctuations. The mechanistic aspects of the essential functionalized electrodes are studied in depth through a variety of spectroscopic and analytical techniques.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference102 articles.

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