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- W3087759519 abstract "Abstract N ‐Alkyl‐ N‐( 2‐(1‐arylvinyl)aryl)cinnamamides are converted into natural product inspired scaffolds via iridium photocatalyzed intramolecular [2+2] photocycloaddition. The protocol has a broad substrate scope, whilst operating under mild reaction conditions. Tethering four components forming a trisubstituted cyclobutane core builds rapidly high molecular complexity. Our approach allows the design and synthesis of a variety of tetrahydrocyclobuta[ c ]quinolin‐3(1 H )‐ones, in yields ranging between 20–99 %, and with excellent regio‐ and diastereoselectivity. Moreover, it was demonstrated that the intramolecular [2+2]‐cycloaddition of 1,7‐enynes—after fragmentation of the cyclobutane ring—leads to enyne‐metathesis‐like products." @default.
- W3087759519 created "2020-09-25" @default.
- W3087759519 creator A5000890483 @default.
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- W3087759519 creator A5023599993 @default.
- W3087759519 creator A5067475475 @default.
- W3087759519 creator A5070806861 @default.
- W3087759519 date "2021-01-18" @default.
- W3087759519 modified "2023-10-16" @default.
- W3087759519 title "Photocatalyzed Intramolecular [2+2] Cycloaddition of <i>N</i> ‐Alkyl‐ <i>N‐(</i> 2‐(1‐arylvinyl)aryl)cinnamamides" @default.
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- W3087759519 doi "https://doi.org/10.1002/chem.202003641" @default.
- W3087759519 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32955792" @default.
- W3087759519 hasPublicationYear "2021" @default.
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