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Acetic Acid Promoted Redox Annulations with Dual C–H Functionalization

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Figshare2017-05-16 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Acetic_Acid_Promoted_Redox_Annulations_with_Dual_C_H_Functionalization/5008892
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资源简介:
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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2017-05-16
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