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Abstract
AbstractA β‐hydroxy elimination instead of common oxidization to carbonyl group in secondary propargyl alcohols was successfully developed to form 2‐benzyl substituted isoquinoline N‐oxides by a Rhodium‐catalyzed C−H activation and annulation cascade, in which moderate to excellent yields (up to 92%) could be obtained under mild reaction conditions, along with good regioselectivity, broad generality and applicability.magnified image
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