Mild Aryl Ether Formation in the Semisynthesis of the Novel Macrolide Immunosuppressant L-732,531
- 22 August 1998
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (19), 6721-6726
- https://doi.org/10.1021/jo980451q
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Preparation and in vitro activities of naphthyl and indolyl ether derivatives of the FK-506 related immunosuppressive macrolide ascomycinBioorganic & Medicinal Chemistry Letters, 1996
- Preparation and in vitro activity of aryl ether derivatives of the FK-506 related immunosuppressive macrolides ascomycin and L-683,742Bioorganic & Medicinal Chemistry Letters, 1995
- FK‐506–A Novel ImmunosuppressantAnnals of the New York Academy of Sciences, 1993
- Solution structure of FK506 from nuclear magnetic resonance and molecular dynamicsJournal of the American Chemical Society, 1990
- Inhibition of FKBP Rotamase Activity by Immunosuppressant FK506: Twisted Amide SurrogateScience, 1990
- Conversion of one hydroxy group in a diol to a phenyl ether with triphenylbismuth diacetate, a new glycol reaction showing strong axial preference in six-membered ringsThe Journal of Organic Chemistry, 1983
- Preparation, reactions, and physical properties of organobismuth compoundsChemical Reviews, 1982
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- Photochemical reactions of N,N-disubstituted .alpha.-oxoamidesThe Journal of Organic Chemistry, 1978
- Direct conversion of N-methylindoles into indoxyl, oxindole, and dioxindole o-benzoatesThe Journal of Organic Chemistry, 1971