![First report of the application of simple molecular complexes as organo-catalysts for Knoevenagel condensation - RSC Advances (RSC Publishing) DOI:10.1039/C5RA09036A First report of the application of simple molecular complexes as organo-catalysts for Knoevenagel condensation - RSC Advances (RSC Publishing) DOI:10.1039/C5RA09036A](https://pubs.rsc.org/image/article/2015/RA/c5ra09036a/c5ra09036a-s2_hi-res.gif)
First report of the application of simple molecular complexes as organo-catalysts for Knoevenagel condensation - RSC Advances (RSC Publishing) DOI:10.1039/C5RA09036A
![Contribution of Knoevenagel Condensation Products toward the Development of Anticancer Agents: An Updated Review - Tokala - 2022 - ChemMedChem - Wiley Online Library Contribution of Knoevenagel Condensation Products toward the Development of Anticancer Agents: An Updated Review - Tokala - 2022 - ChemMedChem - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/8a7a2f74-cb6d-4471-8ea2-5849b32022fc/cmdc202100736-fig-5001-m.jpg)
Contribution of Knoevenagel Condensation Products toward the Development of Anticancer Agents: An Updated Review - Tokala - 2022 - ChemMedChem - Wiley Online Library
![Catalysts | Free Full-Text | A Highly Efficient Bifunctional Catalyst CoOx/tri-g-C3N4 for One-Pot Aerobic Oxidation–Knoevenagel Condensation Reaction Catalysts | Free Full-Text | A Highly Efficient Bifunctional Catalyst CoOx/tri-g-C3N4 for One-Pot Aerobic Oxidation–Knoevenagel Condensation Reaction](https://pub.mdpi-res.com/catalysts/catalysts-10-00712/article_deploy/html/images/catalysts-10-00712-ag.png?1602229820)
Catalysts | Free Full-Text | A Highly Efficient Bifunctional Catalyst CoOx/tri-g-C3N4 for One-Pot Aerobic Oxidation–Knoevenagel Condensation Reaction
![The Knoevenagel reaction is a carbonyl condensation reaction of an ester with an aldehyde or ketone to yield an \alpha , \beta -unsaturated product. Show the mechanism for the Knoevenagel reaction The Knoevenagel reaction is a carbonyl condensation reaction of an ester with an aldehyde or ketone to yield an \alpha , \beta -unsaturated product. Show the mechanism for the Knoevenagel reaction](https://homework.study.com/cimages/multimages/16/knoevenagel_rn_mchnsm9133950250814996021.gif)