A mechanistic study of the Lewis acid–Brønsted base–Brønsted acid catalysed asymmetric Michael addition of diethyl malonate to cyclohexenone-Reference-Cited by-同舟云学术

A mechanistic study of the Lewis acid–Brønsted base–Brønsted acid catalysed asymmetric Michael addition of diethyl malonate to cyclohexenone

Published:2017 Issue:1 Volume:7 Page:90-101
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Samoilichenko Yuri¹²³,Kondratenko Veronica¹²³,Ezernitskaya Mariam¹²³,Lyssenko Konstantin¹²³,Peregudov Alexander¹²³,Khrustalev Victor¹²³⁴³,Maleev Victor¹²³,Moskalenko Margarita¹²³,North Michael⁵⁶⁷⁸⁹,Tsaloev Alan¹⁰¹¹³,Gugkaeva Zalina T.¹²³,Belokon Yuri¹²³

Affiliation:

1. A. N. Nesmeyanov Institute of Organoelement Compounds

2. Russian Academy of Sciences

3. Russian Federation

4. Peoples' Friendship University of Russia

5. Green Chemistry Centre of Excellence

6. Department of Chemistry

7. The University of York

8. York

9. YO10 5DD UK

10. Chemical Diversity Research Institute

11. Khimki

Abstract

Reaction shown to exhibit biomimetic behaviour.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/CY/C6CY01697A

Reference77 articles.

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2. Design of supramolecular chiral ligands for asymmetric metal catalysis

3. Introduction to Frontiers in Transition Metal Catalyzed Reactions, Chem. Rev., ed. J. A. Gladysz, 2011, vol. 111, pp. 1167–2486

4. Recent advances in cooperative bimetallic asymmetric catalysis: dinuclear Schiff base complexes

5. For reviews see: M.Waser, Progress in the Chemistry of Organic Natural Products. Asymmetric Organocatalysis in Natural Product Syntheses, Springer, New York, 2012

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