Synthesis of C19–C27 Fragment of Ansa Chain Part of Rifamycin S
- 1 January 1989
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 18 (1) , 117-118
- https://doi.org/10.1246/cl.1989.117
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Construction of four consecutive asymmetric centers II. Regioselectiveepoxide-ring opening of γ,δ--epoxy-β-methyl alcohols by alkylationTetrahedron Letters, 1987
- Construction of four consecutive asymmetric centers I. - and - selective epoxydation of β-methyl--homoallylic alcoholsTetrahedron Letters, 1987
- [2,3]Wittig rearrangement of 2′-alkenyloxyacetic acid estersTetrahedron Letters, 1986
- The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereofTetrahedron, 1984
- An efficient method for the alkynylation of oxiranes using alkynyl boranesTetrahedron Letters, 1983
- Synthetic Studies of Rifamycins. V. A Chiral Synthesis of an Ansa-chain Compound for the C-17–C-29 Portion of Rifamycin WBulletin of the Chemical Society of Japan, 1982
- Vanadium-catalyzed epoxidations. 2. Highly stereoselective epoxidations of acyclic homoallylic alcohols predicted by a detailed transition-state modelJournal of the American Chemical Society, 1981
- Further synthetic studies on rifamycin sTetrahedron, 1981
- Studies with trialkylsilyltriflates: new syntheses and applicationsTetrahedron Letters, 1981
- Model studies for the synthesis of quassinoids. 1. Construction of the BCE ring systemThe Journal of Organic Chemistry, 1980