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

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Patel, Bhaven and Hilton, Stephen T. (2014) A Radical-Mediated Approach to the Total Synthesis of Fluorinated Marinoquinoline A and Related Tricyclic and Tetracyclic Congeners. Synlett, 26 (01). pp. 79-83. ISSN 0936-5214

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.

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Title:
A Radical-Mediated Approach to the Total Synthesis of Fluorinated Marinoquinoline A and Related Tricyclic and Tetracyclic Congeners
Creators:
Patel, Bhaven and Hilton, Stephen T.
Identification Number:
10.1055/s-0034-1378614
Official URL:
http://dx.doi.org/10.1055/s-0034-1378614
Date:
7 October 2014
Subjects:
500 Natural Sciences and Mathematics > 540 Chemistry & allied sciences
Department:
School of Human Sciences
Uncontrolled Keywords:
trifluoromethylation, radical reaction, Togni’s reagent, marinoquinoline A, tricyclic heterocycles
Record
URI:
https://repository.londonmet.ac.uk/id/eprint/1041
Item Type:
Article
Depositing User:
Bhaven Patel
Date Deposited:
30 Jun 2016 09:11
Revision:
17
Last Modified:
09 Aug 2019 11:49
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