Radicals in Organic Synthesis: Formation of Carbon-carbon Bonds |
Contents
Halogen donor | 1 |
B ELEMENTARY REACTION STEPS BETWEEN | 13 |
CHAPTER THREE | 36 |
Copyright | |
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acid ACO ACO acrylonitrile addition adduct radicals AIBN alcohols aldehydes alkenes alkyl halides alkyl radicals Angew aromatic compounds aryl attack bond forming reactions Bu3 SnH C-C bond formation carbanions carboxylic cations CH₂ chain reactions Chem chiral centers Citterio cleavage CN CN CO₂ CO₂Et CO₂H CO₂Me cyclization reactions D.H.R. Barton DTBP E.J. Corey electron-poor alkenes electron-rich alkenes electron-withdrawing electrophilic electrophilic radicals Engl esters Free Radicals G.A. Russell Giese give products groups H.J. Schäfer halogen intramolecular ipso substitution J.K. Kochi K.U. Ingold ketones Kolbe electrolysis Minisci NaBH nucleophilic occur OCH3 olefinic oxidation Perkin Trans peroxide radical 11 radical anions radical center radical chain radical chemistry radical cyclization radical precursors radical reactions reactions between radicals reactive recombination reduction regioselectivity ring Rüchardt salts SnBu3 SOMO stereoselectivity substituents syntheses Tetrahedron 1985 Tetrahedron Lett tin hydride tin radical trapped tributyltin tributyltin hydride он