135413-17-1Relevant articles and documents
The stereoselective synthesis of a key intermediate of the trinem antibiotic Sanfetrinem
Ghiron, Chiara,Piga, Elisabetta,Rossi, Tino,Tamburini, Bruno,Thomas, Russell J.
, p. 3891 - 3894 (1996)
By modulating the reactivity of the Lewis acid promoter it was possible to obtain, in a single stereoselective condensation step, the methoxyketone 7, an advanced intermediate in the synthesis of Sanfetrinem GV 104326.
Synthesis and antibacterial activity of 4- and 8-methoxy trinems
Andreotti, Daniele,Rossi, Tino,Gaviraghi, Giovanni,Donati, Daniele,Marchioro, Carla,Di Modugno, Enza,Perboni, Alcide
, p. 491 - 496 (2007/10/03)
The synthesis of all the isomers of 8-methoxy-(9S,10S,12R)-10-(1-hydroxyethyl)-11-oxo-1-azatricyclo-[7.20. 03,8]-undec-2-ene-carboxylates 2 and 4-methoxy-(9R,10S,12R)-10-(1-hydroxyethyl)-11-oxo-1-azatricyclo-[7.2.0 .03,8]-undec-2-ene