![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://pub.mdpi-res.com/molecules/molecules-24-03040/article_deploy/html/images/molecules-24-03040-sch001.png?1571741573)
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. | 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
![The Mukaiyama Aldol Reaction: 40 Years of Continuous Development - Matsuo - 2013 - Angewandte Chemie International Edition - Wiley Online Library The Mukaiyama Aldol Reaction: 40 Years of Continuous Development - Matsuo - 2013 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/6327e6d7-d13b-494c-a2c4-c066176c6283/mfig002.gif)
The Mukaiyama Aldol Reaction: 40 Years of Continuous Development - Matsuo - 2013 - Angewandte Chemie International Edition - Wiley Online Library
![Mukaiyama Aldol Reaction Catalyzed by (Benz)imidazolium-Based Halogen Bond Donors | Catalysis | ChemRxiv | Cambridge Open Engage Mukaiyama Aldol Reaction Catalyzed by (Benz)imidazolium-Based Halogen Bond Donors | Catalysis | ChemRxiv | Cambridge Open Engage](https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/60c74eed842e654e2edb3738/largeThumb/mukaiyama-aldol-reaction-catalyzed-by-benz-imidazolium-based-halogen-bond-donors.jpg)
Mukaiyama Aldol Reaction Catalyzed by (Benz)imidazolium-Based Halogen Bond Donors | Catalysis | ChemRxiv | Cambridge Open Engage
![The Mukaiyama Aldol Reaction: 40 Years of Continuous Development - Matsuo - 2013 - Angewandte Chemie International Edition - Wiley Online Library The Mukaiyama Aldol Reaction: 40 Years of Continuous Development - Matsuo - 2013 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5e528dff-c9c3-4571-b1dc-46ee2aafbe61/mcontent.gif)
The Mukaiyama Aldol Reaction: 40 Years of Continuous Development - Matsuo - 2013 - Angewandte Chemie International Edition - Wiley Online Library
![Diastereoselectivity in Lewis-Acid-Catalyzed Mukaiyama Aldol Reactions: A DFT Study | Journal of the American Chemical Society Diastereoselectivity in Lewis-Acid-Catalyzed Mukaiyama Aldol Reactions: A DFT Study | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja3052975/asset/images/medium/ja-2012-052975_0006.gif)
Diastereoselectivity in Lewis-Acid-Catalyzed Mukaiyama Aldol Reactions: A DFT Study | Journal of the American Chemical Society
![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
![Chiral Brønsted Acid as a True Catalyst: Asymmetric Mukaiyama Aldol and Hosomi–Sakurai Allylation Reactions | Journal of the American Chemical Society Chiral Brønsted Acid as a True Catalyst: Asymmetric Mukaiyama Aldol and Hosomi–Sakurai Allylation Reactions | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.5b04168/asset/images/large/ja-2015-041688_0009.jpeg)
Chiral Brønsted Acid as a True Catalyst: Asymmetric Mukaiyama Aldol and Hosomi–Sakurai Allylation Reactions | Journal of the American Chemical Society
![Asymmetric vinylogous Mukaiyama aldol reaction of isatins under bifunctional organocatalysis: enantioselective synthesis of substituted 3-hydroxy-2-ox ... - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00759D Asymmetric vinylogous Mukaiyama aldol reaction of isatins under bifunctional organocatalysis: enantioselective synthesis of substituted 3-hydroxy-2-ox ... - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00759D](https://pubs.rsc.org/image/article/2018/CC/c8cc00759d/c8cc00759d-s1_hi-res.gif)