4.7 Article

Rhodium(III)-Catalyzed Cascade Reactions of Imines/Imidates with 4-Hydroxy-2-alkynoates to Synthesize Regioselective Furanone-Fused Isoquinoline Scaffolds

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JOURNAL OF ORGANIC CHEMISTRY
卷 86, 期 24, 页码 17965-17974

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c02300

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  1. SERB, New Delhi [EMR/2016/006358]
  2. Indian Institute of Science
  3. DYNARX Pvt. Ltd.
  4. SYNMR Chemicals Pvt. Ltd.
  5. CSIR, New Delhi

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A regioselective synthesis of furanone-fused isoquinoline heterocycles was achieved in a single step using a Rh(III) catalyst, showing good regioselectivity with a wide range of alkynoates. The regioselectivity was guided by steric bulk at the C4 position of the 4-hydroxy-2-alkynoates. The synthetic utility was demonstrated with a model reaction scaled up to 1 g.
A regioselective synthesis of furanone-fused isoquinoline heterocycles is developed in a single step using a Rh(III) catalyst. In this reaction, a cascade C-H activation, regioselective annulation, and lactonization occur in one pot. A wide range of alkynoates was examined, which showed good regioselectivity. The regioselectivity was guided by steric bulk at the C4 position of the 4-hydroxy-2-alkynoates. The synthetic utility was exemplified, and the model reaction was scaled up to a 1 g scale.

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