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Oxidation of aliphatic 2,2-dichloroalkanals by HNO3 in CH2Cl2: An easy and eco-friendly route to the corresponding 2,2-dichloroalkanoic acids
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An efficient route to aliphatic 2,2-dichloroaldehydes via chlorination of aldehydes or alcohols with the system Cl-2/quaternary ammonium chloride
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XXVII Convegno Nazionale della Divisione de Chimica Organica a Trieste, Italy, Sept. 4 - 9, 2001, F. Bellesia, L. De Buyck, M.V. Colucci, F. Ghelfi, E. Libertini, C. Mortalò, K.V. Nikitin, U.M. Pagnoni, C.V. Stevens, Approccio inusuale a erbicidi 3-pirrolin-2-onici a partire da 2-pirrolidinoni clorurati
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XXVII Convegno Nazionale della Divisione de Chimica Organica a Trieste, Italy, Sept. 4 - 9, 2001, F. Bellesia, L. De Buyck, F. Ghelfi, C. Mortalò, U.M. Pagnoni, A. Pinetti, C.V. Stevens, R4N+Cl-/Cl2/CH2Cl2: Un sistema efficace ed economico per la selettiva ?- O ???-clorurazione di aldeidi alifatiche
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Unusual access to 5-methoxy or 5,5-dimethoxy-4-methyl-3-pyrrolin-2-ones from chlorinated 4-methyl-pyrrolidin-2-ones.
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2,2-Dichloroaldehydes and 2,2-dichlorocarboxylic acids from 2-picoline center dot HCl catalyzed chlorination of aldehydes.
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2,2-dichlorination of aldehydes with the 2,6-lutidine center dot HCl/Cl-2/CH2Cl2 system: An environmentally benign process suitable for scale up.
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The influence of benzylic protection and allylic substituents on the CuCl-TMEDA catalyzed rearrangement of N-allyl-N-benzyl-2,2-dihaloamides to gamma-lactams. Application to the stereoselective synthesis of pilolactam.