Resolution of 4-oxoazetidin-2-yl benzoate by inclusion crystallization with an optically active host compound
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
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1. Synthesis and antibacterial activity of (1′R, 5R, 6R)-2-tert-butyl-6-(1′-hydroxyethyl)penem-3-carboxylic acid
2. 4-Benzoyloxy-2-azetidinone, a Convenient Synthon for β - Lactam Intermediates
3. Synthesis of 4-aryl-substituted β-lactam enantiomers by enzyme-catalyzed kinetic resolution
4. Lipase-catalyzed kinetic resolution of 7-, 8- and 12-membered alicyclic β-amino esters and N-hydroxymethyl-β-lactam enantiomers
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2. 8.5 Physical Separations: Chiral Discrimination of Enantiomers by Diastereomeric Complexation with Chiral Host Compounds;Comprehensive Chirality;2012
3. Synthesis, structures and inclusion properties of tetranaphthalides: new macrocyclic clathrate hosts;Tetrahedron;2011-04
4. A Convenient Approach toC2-Chiral 1,1,4,4-Tetrasubstituted Butanetetraols: Direct Alkylation or Arylation of Enantiomerically Pure Diethyl Tartrates;Helvetica Chimica Acta;2010-03
5. Molecular and crystalline structures of three (S)-4-alkoxycarbonyl-2-azetidinones containing long alkyl side chains from synchrotron X-ray powder diffraction data;Acta Crystallographica Section B Structural Science;2009-11-16
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