Synthesis of optically active azetidin-2-ones from L-threonine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Stereocontrolled syntheses of chiral intermediates of thienamycin from threonines
2. Stereospecific Synthesis of D-Isothreonine from L-Threonine
3. A new method for the carbon-extension reactions of azetidin-2-ones at the 4-position
4. Regioselective transformation of internal alkynes to unsymmetrical ketones. Novel routes to key intermediates for the synthesis of carbapenem and carbacephem skeletons
5. 2-(Alkylthio)penem-3-carboxylic acids. IV. Synthesis of (hydroxyethyl)azetidinone precursors to 1-thia analogs of thienamycin.
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1. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
2. Synthesis of 3-Carbamoylβ-LactamsviaManganese(III)-Promoted Cyclization ofN-Alkenylmalonamides;Helvetica Chimica Acta;2013-11
3. Practical synthetic approach to 4-acetoxy-2-azetidinone for the preparation of carbapenem and penem antibiotics;Research on Chemical Intermediates;2011-07-07
4. Synthesis of (1′R,3S,4S)-3-[1′-(tert-Butyldimethylsilyloxy)ethyl]- 4-(cyclopropylcarbonyloxy)azetidin-2-one;European Journal of Organic Chemistry;2006-08
5. α-Amido Sulfones as Stable Precursors of Reactive N-Acylimino Derivatives;Chemical Reviews;2005-10-05
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