Total Synthesis of (±)-Goniomitine via Radical Translocation

Citeable URL: https://ir.library.oregonstate.edu/concern/articles/h415pg16t

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Attribute Name	Values
Creator	Vellucci, Jessica K. Beaudry, Christopher M.
Abstract	The aspidosperma alkaloid goniomitine was synthesized in six steps from 2-ethyl-δ-valerolactam. The convergent strategy features an Ullman coupling to assemble the required carbon atoms. A complexity-generating radical translocation reaction was used to build the indole architecture.
Resource Type	Article
DOI	https://doi.org/10.1021/acs.orglett.5b02277
Date Available	2016-09-08T08:00:07+00:00
Date Issued	2015-09-18
Citation	Vellucci, J. K., & Beaudry, C. M. (2015). Total Synthesis of (±)-Goniomitine via Radical Translocation. Organic Letters, 17(18), 4558-4560. doi:10.1021/acs.orglett.5b02277
Journal Title	Organic Letters
Journal Volume	17
Journal Issue/Number	18
Rights Statement	Copyright Not Evaluated
Funding Statement (additional comments about funding)	This work was supported by the National Science Foundation under Grant Number 1465287.
Publisher	American Chemical Society
Peer Reviewed	Yes
Language	English [eng]
Replaces	http://hdl.handle.net/1957/58404

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