Matches in SemOpenAlex for { <https://semopenalex.org/work/W16133025> ?p ?o ?g. }
- W16133025 endingPage "1067" @default.
- W16133025 startingPage "1031" @default.
- W16133025 abstract "The reactions of keto-carbenes (1) or -carbenoids with CC π-bonds1−7 offer a direct entry to highly functionalized cyclopropanes (2),8 which, due to their lability, are readily transformed to a range of products (Scheme 1). The cyclopropanation is often highly stereoselective and further reaction can lead to products of defined stereochemistry, controlled by the compact arrangement of functionality within the cyclopropane ring. Although free carbenes undergo additions to alkenes, these reactions are unselective and competing carbene rearrangements tend to occur. Consequently, metal-stabilized ketocarbenoids, generally formed by catalyzed decomposition of diazo compounds, are of much greater synthetic utility and will be the emphasis of this chapter." @default.
- W16133025 created "2016-06-24" @default.
- W16133025 creator A5083948798 @default.
- W16133025 date "1991-01-01" @default.
- W16133025 modified "2023-10-16" @default.
- W16133025 title "Addition of Ketocarbenes to Alkenes, Alkynes and Aromatic Systems" @default.
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