Author:
Alexander Roger G.,Southgate Robert
Publisher
Royal Society of Chemistry (RSC)
Cited by
23 articles.
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1. Strategies for the Stereocontrolled Formation of Oxygen Analogues of Penicillins and Cephalosporins;Current Medicinal Chemistry;2004-07-01
2. Olivanic acid analogues. Part 7. Lead tetra-acetate oxidation of 3-alkylthio-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylates;Journal of the Chemical Society, Perkin Transactions 1;1990
3. Olivanic acid analogues. Part 5. Synthesis of 3-alkylthio and 3-alkylsulphinyl analogues via Michael addition of thiols to 3-unsubstituted 1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates. X-Ray molecular structure of (2RS,3RS,5SR)-benzyl 3-ethylthio-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylate and (2RS,3SR,5SR,6RS,1′RS)- and (2RS,3SR,5RS,6SR,1′SR)-benzyl 3-chloro-6-(1-hydroxyethyl)-7-oxo-3-[(SR)-phenylsulphinyl]-1-azabicyclo[3.2.0]heptane-2-carboxylate;J. Chem. Soc., Perkin Trans. 1;1990
4. Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions. Part 10. The 9-oxo-6-thia-1,3-diazabicyclo[5.2.0]nonene, 8-oxo-5-thia-1,3-diazabicyclo[4.2.0]octene, and 8-oxo-5-oxa-1,3-diazabicyclo[4.2.0]octene ring systems;J. Chem. Soc., Perkin Trans. 1;1986
5. Synthesis of the 3-acetoxy-7-oxo-1-azabicyclo [3.2.0] hept-2-ene-2-carboxylate system;Tetrahedron Letters;1986-01