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Beilstein J. Org. Chem. 2016, 12, 1072–1078, doi:10.3762/bjoc.12.101
Graphical Abstract
Scheme 1: Selected benzothiadaiazine 1,1-dioxides with potent biological activities.
Scheme 2: Scope of acetophenones (reaction conditions: 1 (0.33 mmol), 2a (0.3 mmol), DMSO (2 mL), I2 (0.75 eq...
Scheme 3: Scope of 2-aminobenzenesulfonamides (reaction conditions: 1 (0.33 mmol), 2a (0.3 mmol), DMSO (2 mL)...
Scheme 4: Reactions of 2-aminobenzenesulfonamides bearing an alknyl group (reaction conditions: 1 (0.33 mmol)...
Scheme 5: Gram scale reaction between 1a and 2a.
Figure 1: X-ray crystal structure of 4b (CCDC 1444753).
Scheme 6: Control experiment.
Scheme 7: Proposed mechanism.
Beilstein J. Org. Chem. 2012, 8, 534–538, doi:10.3762/bjoc.8.61
Scheme 1: Michael addition under catalyst- and solvent-free conditions.
Figure 1: The grinding effect of different grinding aids. Conditions: β-nitrostyrene (14.9 mg, 0.1 mmol), 1,3...
Figure 2: Yields of the model reaction in different solvents. Conditions: β-nitrostyrene (14.9 mg, 0.1 mmol),...
Figure 3: The effect of the amount of quartz sand on the yield. Conditions: β-nitrostyrene (14.9 mg, 0.1 mmol...
Beilstein J. Org. Chem. 2008, 4, No. 40, doi:10.3762/bjoc.4.40
Scheme 1: Simple copper salt-catalyzed N-arylation reaction of amines, amides, imides and sulfonamides.
Scheme 2: N-arylation reaction of phthalimide with arylboroxine.