An intramolecular addition-elimination strategy for the synthesis of carbapenems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. ChemInform Abstract: Intramolecular Addition-Elimination Strategy for the Synthesis of Carbapenems.;ChemInform;2010-08-18
2. Synthesis of 4-allenyl and 4-proparyl-2-azetidinone via Zn-mediated Barbier-type reaction and Pt-catalyzed intramolecular amidation to carbapenem skeletons;Tetrahedron Letters;2007-11
3. EFFICIENT SYNTHESIS OF ORAL THF 1β-METHYLCARBAPENEM (OCA-983) VIA THE WITTIG PROCESS;Synthetic Communications;2001-01
4. General stereoselective synthesis of (E)-exo-alkylidene tetrahydrofurans via base-mediated cyclization of hydroxyl propargylic sulfones;Tetrahedron;1998-10
5. Alkyne−Co2(CO)6 Complexes in the Synthesis of Fused Tricyclic β-Lactam and Azetidine Systems,1;The Journal of Organic Chemistry;1998-09-15
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