Concise synthesis of ketoallyl sulfones through an iron-catalyzed sequential four-component assembly
Mar 092018
Concise synthesis of ketoallyl sulfones through an iron-catalyzed sequential four-component assembly
Green Chem., 2018, 20,973-977
DOI: 10.1039/C7GC03719H, Communication
DOI: 10.1039/C7GC03719H, Communication
Fuhong Xiao, Chao Liu, Dahan Wang, Huawen Huang, Guo-Jun Deng
A three starting material four component reaction (3SM-4CR) strategy is described to prepare [small beta]-acyl allylic sulfones from methyl ketones, sodium sulfinates and dimethylacetamide (DMA) in an iron-catalyzed oxidative system.
A three starting material four component reaction (3SM-4CR) strategy is described to prepare [small beta]-acyl allylic sulfones from methyl ketones, sodium sulfinates and dimethylacetamide (DMA) in an iron-catalyzed oxidative system.
Concise synthesis of ketoallyl sulfones through an iron-catalyzed sequential four-component assembly
Abstract
A three starting material four component reaction (3SM-4CR) strategy is described to prepare β-acyl allylic sulfones from methyl ketones, sodium sulfinates and dimethylacetamide (DMA) in an iron-catalyzed oxidative system. In this process, DMA was used as a dual synthon to provide two carbons. A broad range of functional groups were tolerated in this reaction system.
1-phenyl-2-(tosylmethyl)prop-2-en-1-one (3ab)
43.2 mg, 72% yield).
1 H NMR (400 MHz, CDCl3) δ 7.78 (d, J = 8.2 Hz, 2H), 7.68-7.65 (m, 2H), 7.55 (t, J = 7.4 Hz, 1H), 7.43 (t, J = 7.8 Hz, 2H), 7.30 (d, J = 8.3 Hz, 2H), 6.25 (s, 1H), 6.02 (s, 1H), 4.35 (s, 2H), 2.39 (s, 3H).
13C NMR (100 MHz, CDCl3) δ 194.7, 144.9, 136.1, 135.8, 135.7, 133.9, 132.6, 129.8, 129.6, 128.3, 128.2, 57.7, 21.6.
HRMS calcd. for: C17H17O3S+ [M+H]+ 301.08929, found 301.08908
1H NMR PREDICT
13C NMR PREDICT ABOVE
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Cc1ccc(cc1)S(=O)(=O)CC(=C)C(=O)c2ccccc2
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