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- W4251777405 abstract "Abstract The concept of noncovalent organocatalysis by means of networks of cooperative hydrogen bonds (NCHB organocatalysis) has been explored. Arylideneureas were chosen as ideal substrates because of their powerful donor–acceptor properties. We have examined their uncatalyzed, direct Mannich reaction with acetoacetates in comparison with that catalyzed by a number of salan derivatives capable of providing a network of cooperative hydrogen bonds. Catalyst D [( R , R )‐ N , N ′‐bis(salicyl)cyclohexane‐1,2‐diamine] was found to drive the above direct Mannich reaction in an enantioselective manner, thereby allowing the synthesis of several Biginelli dihydropyrimidinones with high enantioselectivity. DFT calculations (B3LYP‐D‐PCM/6‐31+G*//B3LYP/6‐31+G*) revealed that the NCHB organocatalyst lowers the energy barrier of the reaction. The NCHB organocatalysts appear to function as biomimetic catalysts." @default.
- W4251777405 created "2022-05-12" @default.
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- W4251777405 date "2016-02-25" @default.
- W4251777405 modified "2023-10-18" @default.
- W4251777405 title "Organocatalysis by Networks of Cooperative Hydrogen Bonds: Enantioselective Direct Mannich Addition to Preformed Arylideneureas" @default.
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- W4251777405 doi "https://doi.org/10.1002/ange.201511555" @default.
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