The combination of TsNBr2/TsNH2 as the nitrogen/halo source for the aminobromination of β-methyl-β-nitrostyrenes catalyzed by Mn(OAc)2
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference66 articles.
1. A New Class of Conformationally Rigid Analogues of 4-Amino-5-halopentanoic Acids, Potent Inactivators of γ-Aminobutyric Acid Aminotransferase
2. The cinnamate-based aminohalogenation provides an easy access to anti methyl 3-aryl-N-p-tosyl- and N-o-nosyl-aziridine-2-carboxylates
3. Functionalization of α,β-Unsaturated Esters and Ketones: A Facile and Highly Stereoselective One-Pot Approach to N-Protected α,β-Dehydroamino Acid Derivatives
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1. A Metal-Free Protocol for Aminofunctionalization of Olefins Using TsNBr2;The Journal of Organic Chemistry;2016-06-20
2. Use of Bromine and Bromo-Organic Compounds in Organic Synthesis;Chemical Reviews;2016-05-20
3. N,N-Dibromo-p-Toluenesulfonamide (TsNBr2): A Promising Alternative Bromo-Organic Reagent;Synlett;2016-04-14
4. Metal-Free Amidation of Ethers with N,N-Dibromosulfonamides;Synlett;2016-02-08
5. Unexpected C-C bond cleavage ofα-nitroketone in the presence of TsNBr2: A new pathway for C-N bond formation;Synthetic Communications;2015-12-29
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