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C3-Cyanation of Pyridines: Constraints on Electrophiles and Determinants of Regioselectivity.
Zhang M, Zhou Q, Luo H, Tang ZL, Xu X, Wang XC. Zhang M, et al. Angew Chem Int Ed Engl. 2023 Feb 1;62(6):e202216894. doi: 10.1002/anie.202216894. Epub 2023 Jan 9. Angew Chem Int Ed Engl. 2023. PMID: 36517651
Here, we report a method for C3-selective cyanation of pyridines by a tandem process with the reaction of an in situ generated dihydropyridine with a cyano electrophile as the key step. The method is suitable for late-stage functionalization of pyridine drugs. ...
Here, we report a method for C3-selective cyanation of pyridines by a tandem process with the reaction of an in situ generated dihydropyridi …
Enantioselective Nickel-Catalyzed Hydrosilylation of 1,1-Disubstituted Allenes.
Liu T, Mao XR, Song S, Chen ZY, Wu Y, Xu LP, Wang P. Liu T, et al. Angew Chem Int Ed Engl. 2023 Mar 6;62(11):e202216878. doi: 10.1002/anie.202216878. Epub 2023 Feb 7. Angew Chem Int Ed Engl. 2023. PMID: 36651564
Here, we report the first example of Ni-catalyzed asymmetric hydrosilylation of 1,1-disubstituted allenes with high level of regioselectivities and enantioselectivities. The key to achieve this stereoselective hydrosilylation reaction was the development of the SPSiOL-deri …
Here, we report the first example of Ni-catalyzed asymmetric hydrosilylation of 1,1-disubstituted allenes with high level of regioselectivit …
24 results