Intramolecular C–H arylation of pyridine derivatives with a palladium catalyst for the synthesis of multiply fused heteroaromatic compounds

Yuki Nakanishi, Shoichi Sugita, Kentaro Okano, Atsunori Mori, Ian Baxendale · 2024

Read Intramolecular C–H arylation of pyridine derivatives with a palladium catalyst for the synthesis of multiply fused heteroaromatic compounds by Yuki Nakanishi, Shoichi Sugita, Kentaro Okano, Atsunori Mori, Ian Baxendale (2024) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-11650519.txt.

Description

Yuki Nakanishi and co-authors fuse ring systems with a palladium catalyst in a 2024 study. Building multiply fused heteroaromatic compounds matters for drugs and materials, and direct carbon-hydrogen links promise shorter routes. Their test case joins a brominated amide to its own pyridine ring.

With a palladium salt at high heat, the ring closed in modest yield. Adding a phosphine ligand more than doubled the yield to near total. Cousin amides from several pyridine acids closed in good yields too. Even non-pyridine amides gave fused products above eighty percent. The method widens the fused-ring toolbox.

Catalog record

CREATORYuki Nakanishi, Shoichi Sugita, Kentaro Okano, Atsunori Mori, Ian Baxendale
YEAR2024
COLLECTIONPAPERS
FORMATTXT
FILE SIZE12 KB
VERSION1.0
LICENSECC BY 4.0
RIGHTSCC BY
SOURCEEurope PMC

Source: https://europepmc.org/articles/PMC11650519

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