One-Pot Photocascade\nCatalysis: Access to Pyrrole\nDerivatives from <i>N</i>‑Arylglycines and Morita–Baylis–Hillman\n(MBH) Acetates

The step-economical synthesis of pyrrole derivatives\nhas posed\na challenge in the field of <i>N</i>-heterocyclic chemistry.\nA novel photocascade catalytic radical S<sub>N</sub>2′-type\nreaction/radical addition/annulation sequence of MBH acetates provides\na straightforward route to pyrrole derivatives by forming new C–C,\nC–N, and CC bonds in one pot, using <i>N</i>-arylglycines as the α-arylaminomethyl radical precursors for\ndouble insertion.

Publication Details

Journal
Figshare
Published
2024-11-18
DOI
https://doi.org/10.1021/acs.orglett.4c04176.s001
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

One-Pot Photocascade\nCatalysis: Access to Pyrrole\nDerivatives from N‑Arylglycines and Morita–Baylis–Hillman\n(MBH) Acetates

Figshare
Radical Photochemical Reactions
article

One-Pot Photocascade\nCatalysis: Access to Pyrrole\nDerivatives from N‑Arylglycines and Morita–Baylis–Hillman\n(MBH) Acetates

article en

Abstract

The step-economical synthesis of pyrrole derivatives\nhas posed\na challenge in the field of <i>N</i>-heterocyclic chemistry.\nA novel photocascade catalytic radical S<sub>N</sub>2′-type\nreaction/radical addition/annulation sequence of MBH acetates provides\na straightforward route to pyrrole derivatives by forming new C–C,\nC–N, and CC bonds in one pot, using <i>N</i>-arylglycines as the α-arylaminomethyl radical precursors for\ndouble insertion.

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Openalex Percentile: Top 72%
Radical Photochemical Reactions
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One-Pot Photocascade\nCatalysis: Access to Pyrrole\nDerivatives from <i>N</i>‑Arylglycines and Morita–Baylis–Hillman\n(MBH) Acetates · Figshare (2024) | TGRS Research Map | TGRS