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- Diversity-oriented general protocol for the synthesis of privileged oxygen scaffolds: pyrones, coumarins, benzocoumarins and naphthocoumarins. Atul Goel, Gaurav Taneja, Ashutosh Raghuvanshi, Ruchir Kant, Prakas R. Maulik
, Org. Biomol. Chem.
, 2013
, 11
, 5239
- Mild electrophilic trifluoromethylthiolation of ketones with trifluoromethanesulfanamide. Wei Wu, Xuxue Zhang, Fang Liang, Song Cao
, Org. Biomol. Chem.
, 2015
, 13
, 6992
- Solvent-controlled highly regio-selective thieno[2,3-b]indole formation under metal-free conditions. Penghui Ni, Bin Li, Huawen Huang, Fuhong Xiao, Guo-Jun Deng
, Green Chem.
, 2017
, 19
, 5553
- Copper-catalyzed aerobic oxygenative cross dehydrogenative coupling of methyl ketones with para-C–H of primary anilines. Xiaochen Ji, Dongdong Li, Xuan Zhou, Huawen Huang, Guo-Jun Deng
, Green Chem.
, 2017
, 19
, 619
- Concise synthesis of ketoallyl sulfones through an iron-catalyzed sequential four-component assembly. Fuhong Xiao, Chao Liu, Dahan Wang, Huawen Huang, Guo-Jun Deng
, Green Chem.
, 2018
, 20
, 973
- Porous barium–organic frameworks with highly efficient catalytic capacity and fluorescence sensing ability. Fuling Liu, Yuwen Xu, Lianming Zhao, Liangliang Zhang, Wenyue Guo, Rongming Wang, Daofeng Sun
, J. Mater. Chem. A
, 2015
, 3
, 21545
- Ammonium iodide-promoted cyclization of ketones with DMSO and ammonium acetate for synthesis of substituted pyridines. Xiaojun Pan, Qiao Liu, Liming Chang, Gaoqing Yuan
, RSC Adv.
, 2015
, 5
, 51183
- Electrochemical reactions. Part II. The structure of an unusual product from the reduction of 1-acetylnaphthalene. J. Grimshaw, E. J. F. Rea
, J. Chem. Soc. C
, 1967
, 2628
- A general and convenient method for the synthesis of 2,4-dinitrobenzyl ketones. Almost unlimited access to 2-substituted 6-nitroindoles from 2,4-dinitrotoluene and aldehydes. Robert Bujok, Marcin Wiszniewski, Piotr Cmoch, Zbigniew Wróbel
, New J. Chem.
, 2018
, 42
, 3260
- Selective catalytic synthesis of α-alkylated ketones and β-alkylated secondary alcohols via hydrogen-borrowing. Md. Bakibillah, Sahin Reja, Kaushik Sarkar, Deboshmita Mukherjee, Rajesh Kumar Das
, New J. Chem.
, 2023
, 47
, 13655