U. Kempin et al., MOENOMYCIN-A - NEW CHEMISTRY THAT ALLOWS TO ATTACH THE ANTIBIOTIC TO REPORTER GROUPS, SOLID SUPPORTS, AND PROTEINS, Tetrahedron, 53(52), 1997, pp. 17669-17690
Moenomycin A (18) on reaction with the diazonium salt derived from bif
unctional (protected) 15 yields the coupling product 19 which on reduc
tion is converted into the moenomycin thiol derivative 21. Thiol 21 ha
s been used to prepare selectively moenomycin dansyl and biotin adduct
s 26 and 28, respectively. This work was performed with the aim to use
moenomycin as a tool for studies of the transglycosylation step in pe
ptidoglycan biosynthesis. (C) 1997 Elsevier Science Ltd.