A chemoenzymatic synthesis of the C10-C19 moiety of fk506
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (23) , 3283-3286
- https://doi.org/10.1016/s0040-4039(00)89044-9
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- FK 506 FOR LIVER, KIDNEY, AND PANCREAS TRANSPLANTATIONThe Lancet, 1989
- Studies of the immunosuppressive agent FK-506: synthesis of an advanced intermediateThe Journal of Organic Chemistry, 1989
- Enantioselective synthesis of the C(18) – C(35) segment of immunosuppressant FK-506 using efficient new methodologyTetrahedron Letters, 1989
- Studies relating to the synthesis of the immunosuppressive agent FK-506: application of the two-directional chain synthesis strategy to the pyranose moietyThe Journal of Organic Chemistry, 1989
- Cobalt(II) chloride-promoted thionation of carbonyl compounds: a simple access to silyl thio ketones and thio aldehydesThe Journal of Organic Chemistry, 1989
- Stereoselective syntheses of FK-506 subunits by the rhodium(I)-catalyzed hdrogenation of dienes. The synthesis and coupling of a C10-C19 fragmentThe Journal of Organic Chemistry, 1989
- A synthesis of the C(1)-C(15) segment of tsukubaenolide (FK 506).Tetrahedron Letters, 1988
- Synthesis of the .alpha.,.beta.-diketo amide segment of the novel immunosuppressive FK506The Journal of Organic Chemistry, 1988
- Structure of FK506, a novel immunosuppressant isolated from StreptomycesJournal of the American Chemical Society, 1987
- FK-506, a novel immunosuppressant isolated from a Streptomyces. II. Immunosuppressive effect of FK-506 in vitro.The Journal of Antibiotics, 1987