4.6 Article

Organophotocatalytic cascade cyclization reactions for the synthesis of cyanoalkyl indole[2,1-a]isoquinolinones

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NEW JOURNAL OF CHEMISTRY
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ROYAL SOC CHEMISTRY
DOI: 10.1039/d3nj03172a

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A visible-light-induced organophotocatalytic reaction has been developed for high-yield synthesis of cyanoalkyl indolo[2,1-a]isoquinolinones through the reaction of cyclobutanone oxime esters with 2-aryl indole derivatives. The reaction utilizes an inexpensive photosensitizer and does not require any additives. It also allows for the incorporation of various functional groups.
Visible-light-induced C-C bond breakage of cyclobutanone oxime esters reacted with 2-aryl indole derivatives to afford a variety of cyanoalkyl indolo[2,1-a]isoquinolinones in high yields was developed. The organophotocatalytic radical cascade cyclization reaction uses an inexpensive photosensitizer without any additives in a simple and scalable set-up, and allows the inclusion of many other functional groups.

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