An enantioselective synthesis of the carzinophilin degradation product (2s,3s) 4-amino-2,3-dihydroxy-3-methylbutyric acid
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (28) , 3299-3302
- https://doi.org/10.1016/s0040-4039(00)98282-0
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Stereocontrolled addition to a penaldic acid equivalent: an asymmetric ofTetrahedron Letters, 1984
- Synthetic studies on carzinophilin A. synthesis of the optically active C.1-C.18 segmentTetrahedron Letters, 1983
- Structure of carzinophilin. 3. Structure elucidation by nuclear magnetic resonance spectroscopy. 1Journal of the American Chemical Society, 1983
- Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutionsPure and Applied Chemistry, 1983
- Studies related to antitumor antibiotics. 28. Structure and function of the antitumor antibiotic carzinophillin A: the first natural intercalative bisalkylatorJournal of the American Chemical Society, 1982
- Synthesis of α-Alkoxy-, α-Aryloxy-, and α-BenzyloxyacetaldehydesSynthesis, 1979
- Studies related to antitumor antibiotics. Part IX. Reactions of carzinophillin with DNA assayed by ethidium fluorescenceCanadian Journal of Biochemistry, 1977
- Structure of Carzinophilin. II. A New Amino Acid and Its Derivative from CarzinophilinCHEMICAL & PHARMACEUTICAL BULLETIN, 1971