269409-64-5Relevant academic research and scientific papers
Recent advances in the synthesis of pamamycin-607
Metz, Peter,Bernsmann, Heiko
, p. 383 - 384 (1999)
Using sultones as crucial intermediates, a short and highly stereoselective synthesis of a precursor of the larger fragment and the methyl ester of the smaller fragment of the macrodiolide pamamycin-607 was achieved.
Toward the synthesis of pamamycin-607
Bernsmann, Heiko,Hungerhoff, Benno,Fechner, Regina,Fr?hlich, Roland,Metz, Peter
, p. 1721 - 1724 (2007/10/03)
Using sultone chemistry, a short and highly enantioselective synthesis of an advanced precursor for the larger hydroxy acid moiety and of the complete smaller hydroxy acid portion of the macrodiolide antibiotic pamamycin-607 has been accomplished. (C) 2000 Elsevier Science Ltd.
