Journal ArticleOPEN ACCESS

A Radical-Mediated Approach to the Total Synthesis of Fluorinated Marinoquinoline A and Related Tricyclic and Tetracyclic Congeners

Synlett (2015) 26(1) 79-83
DOI: 10.1055/s-0034-1378614
22Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A radical-mediated approach to the core structure of fluorinated marinoquinoline A, N-methylated marinoquinoline A and related congeners via the use of Togni's reagent is described.

Author supplied keywords

Cite

CITATION STYLE

APA

Patel, B., & Hilton, S. T. (2015). A Radical-Mediated Approach to the Total Synthesis of Fluorinated Marinoquinoline A and Related Tricyclic and Tetracyclic Congeners. Synlett, 26(1), 79–83. https://doi.org/10.1055/s-0034-1378614

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free