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Removing the superfluous: a supported squaramide catalyst with a minimalistic linker applied to the enantioselective flow synthesis of pyranonaphthoquinones

Removing the superfluous: a supported squaramide catalyst with a minimalistic linker applied to... A continuous flow setup has been implemented for the enantioselective production of a library of pyranonaphthoquinones. This was possible through a sequential two-step process involving a squaramide-catalyzed Michael reaction and oxa-Michael cyclization. A key factor for the success of this methodology was the development of a new, cost-effective polystyrene-supported squaramide. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Catalysis Science & Technology Royal Society of Chemistry

Removing the superfluous: a supported squaramide catalyst with a minimalistic linker applied to the enantioselective flow synthesis of pyranonaphthoquinones

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References (23)

Publisher
Royal Society of Chemistry
Copyright
This journal is © The Royal Society of Chemistry
ISSN
2044-4753
eISSN
2044-4761
DOI
10.1039/c6cy00473c
Publisher site
See Article on Publisher Site

Abstract

A continuous flow setup has been implemented for the enantioselective production of a library of pyranonaphthoquinones. This was possible through a sequential two-step process involving a squaramide-catalyzed Michael reaction and oxa-Michael cyclization. A key factor for the success of this methodology was the development of a new, cost-effective polystyrene-supported squaramide.

Journal

Catalysis Science & TechnologyRoyal Society of Chemistry

Published: Jun 28, 2016

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