276690-11-0Relevant articles and documents
Formal total synthesis of stigmatellin A
Yadav,Revathi,Reddy, B.V. Subba
, p. 3943 - 3946 (2017)
An efficient and stereoselective approach for the formal total synthesis of Stigmatellin A has been described. The key steps involved in this synthesis are desymmetrization of the bicyclic olefin to introduce two methyl and two hydroxyl chiral centers, Fr
Diastereo- and enantioselective total synthesis of stigmatellin A
Enders, Dieter,Geibel, Gunter,Osborne, Simon
, p. 1302 - 1309 (2007/10/03)
Stigmatellin A (1) isolated from the myxobacterium Stigmatella aurantiaca is a powerful inhibitor of electron transport in mitochondria and chloroplasts. The first highly diastereo- and enantioselective total synthesis of this important natural product is