(Z)-selective β-bromination ofN-formyl-α, β-dehydroamino acid esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. Synthesis of β-functionalized α, β-dehydroamino acid derivatives
2. A Facile Synthesis of Methyl 1,5-Disubstituted Imidazole-4-carboxylates
3. A Novel Synthesis of Methyl 1,5-Disubstituted Imidazole-4-carboxylates Using 3-Bromo-2-isocyanoacrylates (BICA)
4. Synthesis of 5-Substituted Methyl 1-Hydroxyimidazole-4-carboxylates and 5-Substituted Methyl 1-Aminoimidazole-4-carboxylates Using 3-Bromo-2-isocyanoacrylates (BICA)
5. A novel synthesis of methyl 5-substituted thiazole-4-carboxylates using 3-bromo-2-isocyanoacrylates (BICA)
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1. Stereoselective Synthesis of Dehydroamino Acids and Its Application to the Synthesis of Nitrogen-containing Natural Products;Journal of Synthetic Organic Chemistry, Japan;2022-04-01
2. Straightforward Synthesis of α-Chloromethylketimines Catalyzed by Gold(I). A Clean Way to Building Blocks;The Journal of Organic Chemistry;2022-02-22
3. Highly Enantioselective Electrophilic α-Bromination of Enecarbamates: Chiral Phosphoric Acid and Calcium Phosphate Salt Catalysts;Journal of the American Chemical Society;2012-06-14
4. Convergent Approach to Nonsymmetrical 2,5-Diester Pyrroles;Synlett;2010-11-25
5. ChemInform Abstract: (Z)-Selective β-Bromination of N-Formyl-α,β- dehydroamino Acid Esters.;ChemInform;2010-08-05
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