Synthesis of an α-(aminooxy)arylacetic ester by the reaction of an α-diazo ester with n-hydroxyphthalimide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Structure-activity Relationships within a Series of C(7)-Substitutedoxyiminocephalosporins Containing the C(3)-Methylaminopyridiniumthiomethyl Substituent. Synthesis and Biological Properties of BRL 57342 and Some Close Analogues.
2. Optical Resolution by Preferential Crystallization of 2-(3,4-Carbonyldioxyphenyl)-2-(phthalimidooxy)acetic Acid, a Key Intermediate of Cephalosporin Antibiotic M-14659
3. Synthesis of a Chiral α-(Aminooxy)arylacetic Ester. II. A Route through a Chiral 2-Hydroxy-2-phenylacetic Acid Derivative
4. Asymmetric transformation of a racemic ?-(phthalimidooxy)arylacetic ester by a combination of preferential crystallization and simultaneous racemization
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2. Rh(II)-Catalyzed Reactions of Diazoesters with Organozinc Reagents;Organic Letters;2015-08-04
3. Hydroxylamine Analogs and Derivatives of Amino Acids. Aminooxy Acids;PATAI'S Chemistry of Functional Groups;2010-09-15
4. ChemInform Abstract: Synthesis of an α-(Aminooxy)arylacetic Ester by the Reaction of an α-Diazo Ester with N-Hydroxyphthalimide.;ChemInform;2010-08-12
5. Degradation of hydroxymaleimide in 2-propanol by irradiation of energetic heavy ions (II)—N2-saturated system;Radiation Physics and Chemistry;2010-08
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