763110-44-7Relevant academic research and scientific papers
Application of a new nucleophilic addition/ring closure (NARC) sequence to the synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids
Fallon, Gary D.,Jones, Eric D.,Perlmutter, Patrick,Selajarern, Walailak
, p. 7435 - 7438 (1999)
A rapid method for the enantioselective construction of 2,8-dioxabicyclo[3.2.1]octanes of relevance to the zaragozic acids, employing a tandem NARC sequence of aldol and intramolecular Wacker reactions, is described.
Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions.
Perlmutter, Patrick,Selajerern, Walailak,Vounatsos, Filisaty
, p. 2220 - 2228 (2007/10/03)
Wacker-type cyclisation reactions provide an effective entry into the dioxabicyclo[3.2.1]octane core of the zaragozic acid analogues.
