193074-08-7Relevant articles and documents
Synthetic studies towards the synthesis of western and eastern chloropeptin I, II subunits
Roussi, Georges,Gonzalez Zamora, Eduardo,Carbonnelle, Annie-Claude,Beugelmans, Rene
, p. 2041 - 2063 (2007/10/03)
The western subunit (16-membered ring) was synthesized by the intramolecular SNAr reaction while the first 16-membered ring compound was obtained as a model of the eastern subunit via an intramolecular Ni0 mediated coupling reaction.
Synthesis of a model of chloropeptins I, II western subunit by the intramolecular S(N)Ar based methodology
Roussi, Georges,Zamora, Eduardo Gonzalez,Carbonnelle, Annie-Claude,Beugelmans, Rene
, p. 4401 - 4404 (2007/10/03)
Formation of a biaryl ether bond between the termini of a tetrapeptide containing a highly racemization prone amino acid by the intramolecular SNAr reaction afforded two diastereomeric 16-membered macrocycles along with their respective atropoisomers. The (R,S,R) and its atropoisomer constituted model of chloropeptins I, II, western part.