Bifunctional chiral synthons via biochemical methods, 4. Chiral precursors to (+)-biotin and (−)-a-factor.
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (44) , 4999-5002
- https://doi.org/10.1016/s0040-4039(01)91101-3
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Bifunctional chiral synthons via biochemical methods. III. Optical purity enhancement in enzymic asymmetric catalysisJournal of the American Chemical Society, 1984
- Revision of the absolute configuration of a-factorTetrahedron, 1983
- Synthesis of optically active forms of a-factor the inducer of streptomycin biosynthesis in inactive mutants of streptomyces griseusTetrahedron, 1982
- A new inducer of anthracycline biosynthesis from Streptomyces viridochromogenes.The Journal of Antibiotics, 1982
- Asymmetric hydrolysis of esters by biochemical methods. Part V. Asymmetric hydrolysis of prochiral diesters with pig liver esterase. Preparation of optically active intermediates for the synthesis of (+)-biotin and (+)-.ALPHA.-methyl-3,4-dihydroxyphenylalanine.Agricultural and Biological Chemistry, 1982
- Synthetic studies on polyether antibiotics. 5. Total synthesis of monensin. 2. Stereocontrolled synthesis of the right half of monensinJournal of the American Chemical Society, 1979
- Versuche zur Biotinsynthese. Herstellung von (3aS, 6aR)‐1, 3‐Dibenzyl‐tetrahydro‐4H‐thieno[3, 4‐d]imidazol‐2,4(1H)‐dionHelvetica Chimica Acta, 1970
- Purification and properties of pig liver esteraseArchives of Biochemistry and Biophysics, 1969