A ring-closing enyne metathesis approach to functionalized semicyclic dienes: The total synthesis of (-)-tetrangomycin
The angucycline antibiotic (-)-tetrangomycin was synthesized in 13 steps (11 % overall yield) by using a stereoselective Diels-Alder reaction between a naphthoquinone and a semicyclic diene to construct the benz[a]anthraquinone ring system. The diene inte
Moodie, Lindon W. K.,Larsen, David S.
p. 1684 - 1694
(2014/03/21)
A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin
The angucycline antibiotic (-)-tetrangomycin was synthesized in 13 steps (11 % overall yield) by using a stereoselective Diels-Alder reaction between a naphthoquinone and a semicyclic diene to construct the benz[a]anthraquinone ring system. The diene inte
Moodie, Lindon W. K.,Larsen, David S.
p. 1684 - 1694
(2015/10/05)
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