![Molecules | Free Full-Text | Very Recent Advances in Vinylogous Mukaiyama Aldol Reactions and Their Applications to Synthesis Molecules | Free Full-Text | Very Recent Advances in Vinylogous Mukaiyama Aldol Reactions and Their Applications to Synthesis](https://www.mdpi.com/molecules/molecules-24-03040/article_deploy/html/images/molecules-24-03040-sch001.png)
Molecules | Free Full-Text | Very Recent Advances in Vinylogous Mukaiyama Aldol Reactions and Their Applications to Synthesis
![Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. - Abstract - Europe PMC Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3465709/bin/nihms404156f5.jpg)
Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. - Abstract - Europe PMC
Highly enantioselective Mukaiyama aldol reaction in aqueous conditions using a chiral iron(ii) bipyridine catalyst - Chemical Communications (RSC Publishing)
![The Mukaiyama Aldol addition is another reaction that provides the functionalization of an aldehyde using a silyl enol ether. Draw the mechanism of the product formation and provide a transition state in The Mukaiyama Aldol addition is another reaction that provides the functionalization of an aldehyde using a silyl enol ether. Draw the mechanism of the product formation and provide a transition state in](https://homework.study.com/cimages/multimages/16/mechanism_of_mukaiyama2580175458881219377.png)
The Mukaiyama Aldol addition is another reaction that provides the functionalization of an aldehyde using a silyl enol ether. Draw the mechanism of the product formation and provide a transition state in
![Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. | Semantic Scholar Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0cdc5c71785901234c4a2f240e2fa33c9acae1fe/2-Figure2-1.png)
Diastereoselectivity in Lewis-acid-catalyzed Mukaiyama aldol reactions: a DFT study. | Semantic Scholar
Diastereoselectivity in Lewis-Acid-Catalyzed Mukaiyama Aldol Reactions: A DFT Study | Journal of the American Chemical Society
![Mukaiyama Aldol Reactions in Aqueous Media - Kitanosono - 2013 - Advanced Synthesis & Catalysis - Wiley Online Library Mukaiyama Aldol Reactions in Aqueous Media - Kitanosono - 2013 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/2045e60b-3f12-424d-a20b-557a533dfa55/msch002.jpg)