Mattson Boronate Urea Pinacol Ester
Mattson Boronate Urea Pinacol Ester结构式
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常用名 | Mattson Boronate Urea Pinacol Ester | 英文名 | Mattson Boronate Urea Pinacol Ester |
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| CAS号 | 1538637-10-3 | 分子量 | 474.20 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C21H21BF6N2O3 | 熔点 | 230.39°C | |
| MSDS | 美版 | 闪点 | N/A |
| 英文名 | Mattson Boronate Urea Pinacol Ester |
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| 英文别名 | 更多 |
| 熔点 | 230.39°C |
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| 分子式 | C21H21BF6N2O3 |
| 分子量 | 474.20 |
| 储存条件 | 2-8°C |
| 危险品运输编码 | NONH for all modes of transport |
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Urea-catalyzed N-H insertion-arylation reactions of nitrodiazoesters.
J. Org. Chem. 79(11) , 4832-42, (2014) The power of hydrogen-bond donor catalysis has been harnessed to elicit and control carbene-like reactivity from nitrodiazoesters. Specifically, select ureas have been identified as effective catalyst... |
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Arylation of diazoesters by a transient N-H insertion organocascade.
Angew. Chem. Int. Ed. Engl. 52(43) , 11317-20, (2013) It takes two: A unique organocatalyzed cascade for the unsymmetric double arylation of α-nitrodiazoesters is described. This organocascade features the strategic use of carbene-activating anilines in ... |
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Urea-catalyzed construction of oxazinanes.
Org. Biomol. Chem. 11(35) , 5793-7, (2013) Highly functionalized oxazinanes are efficiently prepared through urea-catalyzed formal [3 + 3] cycloaddition reactions of nitrones and nitrocyclopropane carboxylates. The reaction system is general w... |
| MFCD22570856 |
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