Total synthesis of (-)-archazolid B.

The archazolids are complex polyketides isolated from the myxobacterium Archangium gephyra and are potent inhibitors of vacuolar type ATPases. Herein, we report the first total synthesis of archazolid A, which establishes unequivocally the relative and absolute configuration of this macrolide antibiotic. Key features of our synthesis include an aldol condensation for construction of the delicate (Z,Z,E)-triene-system, an E-selective Heck reaction on a highly elaborate substrate, and a HWE macrocyclization to close the 24-membered macrolactone.

[1]  Jun Li,et al.  Total synthesis of archazolid A. , 2007, Journal of the American Chemical Society.

[2]  C. Farés,et al.  Stereochemical determination of Archazolid A and B, highly potent vacuolar-type ATPase inhibitors from the Myxobacterium Archangium gephyra. , 2006, Organic letters.

[3]  D. J. Wallace Relay ring-closing metathesis-a strategy for achieving reactivity and selectivity in metathesis chemistry. , 2005, Angewandte Chemie.

[4]  T. Hoye,et al.  Relay ring-closing metathesis (RRCM): a strategy for directing metal movement throughout olefin metathesis sequences. , 2004, Journal of the American Chemical Society.

[5]  E. J. Bowman,et al.  Total synthesis of the salicylate enamide macrolide oximidine III: application of relay ring-closing metathesis. , 2004, Angewandte Chemie.

[6]  H. Reichenbach,et al.  Archazolids, new cytotoxic macrolactones from Archangium gephyra (Myxobacteria). Production, isolation, physico-chemical and biological properties. , 2003, The Journal of antibiotics.

[7]  D. Trauner,et al.  Synthetic studies toward SNF4435 C and SNF4435 D. , 2002, Organic letters.

[8]  B. Trost,et al.  Total synthesis of deschlorocallipeltoside A. , 2001, Journal of the American Chemical Society.

[9]  H. Brown,et al.  Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes. , 1986, Journal of the American Chemical Society.