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Publikováno v:
Journal of the American Chemical Society.
Herein, we report a multistep one-pot reaction of substituted pyridines leading to N-protected tetrahydropyridines with outstanding enantioselectivity (up to 97% ee). An iridium(I)-catalyzed dearomative 1,2-hydrosilylation of pyridines enables the us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a163d636350b8f3d72c77db6a5760d14
https://doi.org/10.1021/jacs.3c02470
https://doi.org/10.1021/jacs.3c02470
