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- The stability and reactivity of tri-, di-, and monofluoromethyl/methoxy/methylthio groups on arenes under acidic and basic conditions. Lingfei Wang, Jun Wei, Ranran Wu, Gang Cheng, Xinjin Li, Jinbo Hu, Yongzhou Hu, Rong Sheng
, Org. Chem. Front.
, 2017
, 4
, 214
- Friedel–Crafts sulfonylation of aromatics catalysed by solid acids: An eco-friendly route for sulfone synthesis. Boyapati M. Choudary, N. Sreenivasa Chowdari, M. Lakshmi Kantam
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2689
- Expeditious entry into carbocyclic and heterocyclic spirooxindoles. Madhu Ganesh, Shammy Suraj
, Org. Biomol. Chem.
, 2022
, 20
, 5651
- Synthesis of sulfones using sodium perchlorate as a catalyst under neutral conditions. B. P. Bandgar, V. T. Kamble, D. B. Fulse, M. V. Deshmukh
, New J. Chem.
, 2002
, 26
, 1105
- Efficient synthesis of aliphatic sulfones by Mg mediated coupling reactions of sulfonyl chlorides and aliphatic halides. Ying Fu, Qin-Shan Xu, Quan-Zhou Li, Zhengyin Du, Ke-Hu Wang, Danfeng Huang, Yulai Hu
, Org. Biomol. Chem.
, 2017
, 15
, 2841
- A three-component reaction of arynes, sodium sulfinates, and aldehydes toward 2-sulfonyl benzyl alcohol derivatives. Yifan Hu, Yuanting Huang, Xi Zhao, Yang Gao, Xianwei Li, Qian Chen
, Org. Biomol. Chem.
, 2021
, 19
, 7066
- Sulfoxidation on a SiO2-supported Ru complex using O2/aldehyde system. Niladri Maity, Chularat Wattanakit, Satoshi Muratsugu, Nozomu Ishiguro, Yong Yang, Shin-ichi Ohkoshi, Mizuki Tada
, Dalton Trans.
, 2012
, 41
, 4558
- CuI promoted sulfenylation of organozinc reagents with arylsulfonyl chlorides. Ying Fu, Yuhu Su, Qin-shan Xu, Zhengyin Du, Yulai Hu, Ke-Hu Wang, Danfeng Huang
, RSC Adv.
, 2017
, 7
, 6018
- N–S bond cleavage of tosyl hydrazones by dual reactive arynes: synthesis of diaryl sulfones, spiro[indazole-3,3′-indolin]-2′-one, and N-phenyl sulfonohydrazides. Suresh Snoxma Smile, Ponnusamy Shanmugam
, New J. Chem.
, 2023
, 47
, 3856
- Preparation of 4-arylquinazolines with o-(N-alkyl,N-p-tosyl)aminobenzonitriles, aryllithiums, and NIS. Hiroki Naruto, Hideo Togo
, Org. Biomol. Chem.
, 2020
, 18
, 5666