Carbocatalysis expands its applicability to the synthesis of indenes via intramolecular Friedel-Crafts like alkylation of Morita-Baylis-Hilman alcohols. Graphene oxide (GO) dictated the conditions to document a C−C bond forming protocol fe...
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Enantioselective Construction of Axially Iodobenzocarbazole Derivatives via Stereogenic‐at‐cobalt(III)‐complex‐catalyzed Iodoarylation of Alkynes
Von Wiley-VCH zur Verfügung gestellt
A new synthetic approach to novel axially chiral iodobenzocarbazole derivatives based on the highly enantioselective intramolecular iodoarylation of linked alkyne−indole systems was developed by using the versatile chiral catalyst, Stereogenic-at-cobalt(III) complex, through an axially chiral iodinated vinylidene o-quinone methide (IVQM) intermediate. This protocol provides 21 examples in excellent yields with good to high enantioselectivities (up to 96% yield, 98% ee). Furthermore, the introduced iodine atoms can easily be converted into other functional groups.
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