Electrochemical\nSelenized Reaction of <i>N</i>‑Arylbicyclo[1.1.0]butane-1-carboxamides:\nAccess to 3‑(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one\nDerivatives

A novel selenized reaction of <i>N</i>-arylbicyclo\n[1.1.0]butane-1-carboxamides\nwith diselenide for the synthesis of polycyclic indoline derivatives\nis developed under electrochemical conditions. The synthesis is achieved\nby the bicyclo[1.1.0]butane strain-release reaction and intramolecular\ncyclization process. In addition, this approach features a wide range\nof substrates, good group tolerance, shorter reaction time, and mild\nconditions.

Publication Details

Journal
Figshare
Published
2024-10-23
DOI
https://doi.org/10.1021/acs.joc.4c02085.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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article

Electrochemical\nSelenized Reaction of N‑Arylbicyclo[1.1.0]butane-1-carboxamides:\nAccess to 3‑(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one\nDerivatives

Figshare
Mycorrhizal Fungi and Plant Interactions
article

Electrochemical\nSelenized Reaction of N‑Arylbicyclo[1.1.0]butane-1-carboxamides:\nAccess to 3‑(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one\nDerivatives

article en

Abstract

A novel selenized reaction of <i>N</i>-arylbicyclo\n[1.1.0]butane-1-carboxamides\nwith diselenide for the synthesis of polycyclic indoline derivatives\nis developed under electrochemical conditions. The synthesis is achieved\nby the bicyclo[1.1.0]butane strain-release reaction and intramolecular\ncyclization process. In addition, this approach features a wide range\nof substrates, good group tolerance, shorter reaction time, and mild\nconditions.

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Openalex Percentile: Top 63%
Mycorrhizal Fungi and Plant Interactions
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Electrochemical\nSelenized Reaction of <i>N</i>‑Arylbicyclo[1.1.0]butane-1-carboxamides:\nAccess to 3‑(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one\nDerivatives · Figshare (2024) | TGRS Research Map | TGRS