923027-62-7Relevant academic research and scientific papers
Total synthesis of (+)-acutiphycin
Moslin, Ryan M.,Jamison, Timothy F.
, p. 9736 - 9745 (2008/03/17)
(Chemical Equation Presented) Synthetic studies toward the total synthesis of (+)-acutiphycin (1) resulted in the discovery of additive-free, highly regioselective nickel-catalyzed reductive coupling reactions of aldehydes and 1,6-enynes and the construct
Toward the total synthesis of lophotoxin - New methodologies and synthetic strategies
Wipf, Peter,Grenon, Michel
, p. 1226 - 1241 (2007/10/03)
Our recent progress toward the synthesis of the furanocembranolide lophotoxin (1) is disclosed. Strategies for the stereoselective incorporation of the C13 stereocenter by a catalytic desymmetrization of a cyclic meso-anhydride, as well as a no
Highly convergent total synthesis of (+)-acutiphycin
Moslin, Ryan M.,Jamison, Timothy F.
, p. 15106 - 15107 (2007/10/03)
An enantioselective, convergent, total synthesis of (+)-acutiphycin (18 steps, longest linear sequence from commercial materials) features the first application of an alkynyl ether as a macrolactone precursor in total synthesis, as well as the first examp
