Journal
ORGANIC LETTERS
Volume 25, Issue 26, Pages 4808-4812Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c01509
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An efficient method for the synthesis of bipyrroles with an axially chiral N-N bond has been developed using a rhodium-catalyzed C-H bond insertion reaction. The desired atropisomers were obtained in high yields (up to 97%) and with excellent enantioselectivities (up to 99% ee).
An atroposelective synthesis of bipyrroleswith an axially chiralN-N bond has been established via a rhodium-catalyzed C-Hbond insertion reaction to provide the desired atropisomers in goodyields (up to 97% yield) with good to excellent enantioselectivities(up to 99% ee).
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