Domino Michael/Michael reaction catalyzed by switchable modularly designed organocatalysts-Reference-Cited by-同舟云学术

Domino Michael/Michael reaction catalyzed by switchable modularly designed organocatalysts

Published:2022 Issue:1 Volume:20 Page:163-172
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Parella Ramarao¹,Jakkampudi Satish¹,Bora Pranjal¹,Sakkani Nagaraju¹^ORCID,Zhao John C.-G.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Texas at San Antonio, One UTSA Circle, San Antonio, Texas 78249-069, USA

Abstract

Both the enamine and iminium catalysis of the MDOs are switchable. Upon switching on both catalytic modes, the MDOs were used for catalyzing the domino Michael/Michael reaction between (E)-7-aryl-7-oxohept-5-enals and trans-cinnamaldehydes.

Funder

Welch Foundation

Division of Chemistry

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D1OB01991K

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