期刊
SYNTHESIS-STUTTGART
卷 -, 期 -, 页码 -出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0042-1751424
关键词
acrylamides; difunctionalization of alkenes; photocatalysis; chlorosulfonylation; alpha-chlorosulfones
A one-step chlorosulfonylation of acrylamides via a photo-catalytic redox process is reported, which provides α-chlorosulfonylamides with a quaternary center in high regioselectivity through radical process. This method is applicable to a broad range of substrates and affords the products in moderate to good yields.
A one-step chlorosulfonylation of acrylamides via a photo-catalytic redox process is described. This reaction provides a-chlorosul-fonylamides with a quaternary center with high regioselectivity via radi-cal process. It is amenable to a broad range of substrates and the products are obtained in moderate to good yields.
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