Carbanion methodology for alkylations and acylations in the synthesis of substituted oxazoles. The formation of Cornforth rearrangement products.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Oxazoles and Their Benzo Derivatives;Boyd,1984
2. A general, one-pot method for the synthesis of 2-substituted oxazoles
3. Synthesis of poly-oxazole systems found in marine metabolites
4. Generation and use of a zinc derivative of a functionalized 1,3-oxazole. Solution of the virginiamycin/madumycin oxazole problem
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1. A general and practical route to 4,5-disubstituted oxazoles using acid chlorides and isocyanides;RSC Advances;2015
2. Total Synthesis of (+)-Ileabethoxazole via an Iron-Mediated Pauson–Khand [2 + 2 + 1] Carbocyclization;Journal of the American Chemical Society;2014-06-04
3. 3.03 Alkylation of α-Sulfur-Containing Carbanions;Comprehensive Organic Synthesis II;2014
4. Synthesis and transformations of derivatives of 2-aryl-5-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3-oxazole-4-carboxylic acid;Russian Journal of General Chemistry;2010-11
5. Cornforth Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15
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