354563-56-7Relevant academic research and scientific papers
Evaluation of possible intramolecular [4+2] cycloaddition routes for assembling the central tetracyclic core of the potent marine antiinflammatory agent mangicol A
Pichlmair, Stefan,de Lera Ruiz, Manuel,Basu, Kallol,Paquette, Leo A.
, p. 5178 - 5194 (2007/10/03)
A plan for enantioselective construction of the mangicol A framework by means of intramolecular Diels-Alder cycloaddition is outlined. First to be assembled is the enantiopure cyclopentenecarboxylic acid 16. Of the several approaches targeting the 1,3-die
Sulfenamide catalyzed oxidation of alcohols to the corresponding carbonyl compounds with anhydrous chloramine-T.
Kitagawa, Hideo,Mukaiyama, Teruaki
, p. 1276 - 1279 (2007/10/03)
N-tert-Butylbenzenesulfenamide (1) catalyzed oxidation of various alcohols with stoichiometric amount of anhydrous chloramines-T (2) proceeded smoothly at room temperature to afford the corresponding carbonyl compounds in good yields.
