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Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization.

ABSTRACT: 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.

SUBMITTER: Zhu Z

PROVIDER: S-EPMC5460294 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization.

Zhu Zhengbo Z Seidel Daniel D

Organic letters 20170516 11

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. ...[more]

PMID: 28510444

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