256327-75-0Relevant articles and documents
Total synthesis of everninomicin 13,384-1 - Part 1: Retrosynthetic analysis and synthesis of the A1B(A)C fragment
Nicolaou,Rodriguez, Rosa Maria,Mitchell, Helen J.,Suzuki, Hideo,Fylaktakidou, Konstantina C.,Baudoin, Olivier,Van Delft, Floris L.
, p. 3095 - 3115 (2007/10/03)
In this first of a series of four articles we introduce everninomicin 13,384-1 (1), a powerful antibiotic effective against drug resistant bacteria, as a target for total synthesis and discuss its retrosynthetic analysis. From the three defined fragments required for the synthesis (2: A1B(A)C fragment; 4: DE fragment; 5: FGHA2 fragment), we describe herein two approaches to the A1B(A)C block. The first strategy relied on an olefin metathesis reaction to construct a common intermediate for rings B and C, but was faced with final protecting group problems. The second, and successful approach, involved a 1,2-phenylsulfeno migration and a sulfur directed glycosidation procedure to link rings B and C, as well as an acyl fluoride intermediate to install the sterically hindered aryl ester moiety (ring A1). The final stages of the synthesis of the required 2-phenylseleno glycosyl fluoride 2 required introduction of a phenylseleno group at C-1 of ring C followed by a novel, DAST-promoted 1,2-migration to produce the desired 2-β-phenylseleno glycosyl fluoride moiety.
Stereocontrolled synthesis of the everninomicin A1B(A)C ring framework
Nicolaou,Rodriguez, Rosa M.,Mitchell, Helen J.,Van Delft, Floris L.
, p. 1874 - 1876 (2007/10/03)
A strategy based on a ring-closing olefin metathesis was used to convert divinylmethanol into 1, which served as a common precursor to activated derivatives 2 and 3. These in turn serve as precursors to the C and B carbohydrate units of the A1B
