Studies towards the total synthesis of rapamycin: A convergent and stereoselective synthesis of the C 22 C 32 carbon framework
JC Anderson, SV Ley, SP Marsden
Index: Anderson, James C.; Ley, Steven V.; Marsden, Stephen P. Tetrahedron Letters, 1994 , vol. 35, # 13 p. 2087 - 2090
Full Text: HTML
Citation Number: 37
Abstract
Abstract A convergent synthesis of the C 22 C 32 portion of rapamycin has been achieved by way of a Nozaki-Kishi coupling of vinyl iodide 14 with aldehyde 13. This aldehyde is available by the stereoselective addition of organometallic reagents to aldehyde 5, synthesised by either of two selenium mediated electrophilic cyclisations. Optically active starting materials for this synthesis are prepared by an enzymatic acylation of meso-diol 6.
Related Articles:
[Ley, Steven V.; Tackett, Miles N.; Maddess, Matthew L.; Anderson, James C.; Brennan, Paul E.; Cappi, Michael W.; Heer, Jag P.; Helgen, Celine; Kori, Masakuni; Kouklovsky, Cyrille; Marsden, Stephen P.; Norman, Joanne; Osborn, David P.; Palomero, Maria A.; Pavey, John B. J.; Pinel, Catherine; Robinson, Lesley A.; Schnaubelt, Juergen; Scott, James S.; Spilling, Christopher D.; Watanabe, Hidenori; Wesson, Kieron E.; Willis, Michael C. Chemistry - A European Journal, 2009 , vol. 15, # 12 p. 2874 - 2914]