Acetic Acid Promoted Redox Annulations with Dual C–H Functionalization
نویسندگان
چکیده
Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-alkylquinoline-3-carbaldehydes as well as the corresponding 4-alkyl isomers and pyridine analogues. These processes involve dual C-H bond functionalization. Acetic acid is used as a cosolvent and acts as the sole promoter of these transformations.
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عنوان ژورنال:
دوره 19 شماره
صفحات -
تاریخ انتشار 2017