A facile method for the preparation of 6-epi-penicillins
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (4) , 285-287
- https://doi.org/10.1016/s0040-4039(01)84302-1
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Equilibration of penicillanic acid derivativesJournal of the Chemical Society D: Chemical Communications, 1971
- Epimerisation of penicillanic acid derivatives and their rearrangement to 1,4-thiazepines: evidence for an E1cB mechanismJournal of the Chemical Society D: Chemical Communications, 1971
- 6-Epi-penicillins and 7-epi-cephalosporinsTetrahedron Letters, 1970
- On the conditions for C-6 epimerization of the penicillin nucleus by a β-elimination mechanismJournal of the Chemical Society D: Chemical Communications, 1970
- A novel rearrangement of a penicillanic acid derivativeJournal of the Chemical Society D: Chemical Communications, 1970
- Epi-6-aminopenicillanic acid and epipenicillin gTetrahedron Letters, 1969
- Structural studies on penicillin derivatives. II. Configuration of phthalimidopenicillin and epiphthalimidopenicillin sulfoxidesJournal of the American Chemical Society, 1969
- EpihetacillinTetrahedron Letters, 1968
- Desaminierung von 6‐AminopenicillansäureHelvetica Chimica Acta, 1967
- The Stereochemistry of Oxidation at Sulfur. Oxidation of 4-Substituted Thianes to Sulfoxides1Journal of the American Chemical Society, 1965