870135-78-7Relevant academic research and scientific papers
Harnessing glycal-epoxide rearrangements: The generation of the AB, EF, and IJ rings of adriatoxin
Osei Akoto, Clement,Rainier, Jon D.
supporting information; experimental part, p. 8055 - 8058 (2009/04/12)
(Chemical Equation Presented) Climbing the ladder: The generation of three bicyclic subunits ofadriatoxin (see structure) was accomplished by using glycal-epoxide rearrangements, glycal-Claisen rearrangements, and C-glycoside-forming reactions.
Rapid two-directional synthesis of the F-J fragment of the gambieric acids by iterative double ring-closing metathesis
Clark, J. Stephen,Kimber, Marc C.,Robertson, Jerod,McErlean, Christopher S. P.,Wilson, Claire
, p. 6157 - 6162 (2007/10/03)
(Chemical Equation Presented) D-glucal is the starting point for the efficient synthesis of the F-J fragment of the gambieric acids (see scheme). The hiring diol was subjected to double two-directional alkynyl ether formation, carbocupration ring-closing
