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pro vyhledávání: '"Mohammad M. Baag"'
Autor:
Simon Biller, Lutz F. Tietze, Mohammad M. Baag, Simone Dietz, Judith Hierold, Nina Schützenmeister, Timo Scheffer
Publikováno v:
European Journal of Organic Chemistry. 2013:7305-7312
For the synthesis of novel spinosyn analogues, the selective introduction of the 2-deoxyamino sugar, D-forosamine, necessary for their bioactivity, is described. The reactions of different alcohol acceptors with the D-forosamine donor in the presence
Autor:
Markus Granitzka, Dietmar Stalke, Nina Schützenmeister, Alexander Grube, Timo Scheffer, Lutz F. Tietze, Mohammad M. Baag
Publikováno v:
European Journal of Organic Chemistry. 2012:5748-5756
New spinosyn analogues 3 with an arene group as ring A and containing a L-rhamnose moiety have been prepared. The key step in the synthesis of 3 is a Pd-catalyzed twofold Heck reaction of glycosylated bromoarene 4, containing an iodovinyl side chain