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- Switchable regioselective hydroalkylation of 2-arylindoles with maleimides. Dhananjay S. Nipate, Vikki N. Shinde, Krishnan Rangan, Anil Kumar
, Org. Biomol. Chem.
, 2021
, 19
, 4910
- Synthesis and biological activity of hydroxybenzylidenyl pyrrolidine-2,5-dione derivatives as new potent inhibitors of tyrosinase. Young Mi Ha, Jin-Ah Kim, Yun Jung Park, Daeui Park, Yeon Ja Choi, Ji Min Kim, Ki Wung Chung, Yu Kyeong Han, Ji Young Park, Ji Yeon Lee, Hyung Ryong Moon, Hae Young Chung
, Med. Chem. Commun.
, 2011
, 2
, 542
- Stereoselective synthesis of trifluoroethyl 3,2′-spirooxindole γ-lactam through the organocatalytic cascade reaction of 3-((2,2,2-trifluoroethyl)amino)indolin-2-one. Shuai-Jiang Liu, Qing Mao, Gu Zhan, Rui Qin, Ben-Hong Chen, Jing Xue, Meng-Lan Luo, Qian Zhao, Bo Han
, Org. Biomol. Chem.
, 2021
, 19
, 467
- Synthesis of maleimide-functionalized carboranes and their utility in Michael addition reactions. Valentina A. Ol'shevskaya, Victoria M. Alpatova, Anton V. Makarenkov, Elena G. Kononova, Alexander F. Smol’yakov, Alexander S. Peregudov, Evgeny G. Rys
, New J. Chem.
, 2021
, 45
, 12159
- Valuable new platform chemicals obtained by valorisation of a model succinic acid and bio-succinic acid with an ionic liquid and high-pressure carbon dioxide. Daniel Silva, Ewa Bogel-Łukasik
, Green Chem.
, 2017
, 19
, 4048
- Unusual polymorphs of rac-3-phenylpyrrolidine-2,5-dione with Z′ = 1, 2, and 3. Tatiana V. Timofeeva, Victoria Sena, Boris B. Averkiev, Shabari N. Bejagam, Muhammad Usman, Arcadius V. Krivoshein
, CrystEngComm
, 2019
, 21
, 6819
- Synthesis, X-ray powder diffraction and DFT calculations of vasorelaxant active 3-(arylmethylidene)pyrrolidine-2,5-diones. ElSayed M. Shalaby, Adel S. Girgis, Hanaa Farag, Ahmed F. Mabied, Andrew N. Fitch
, RSC Adv.
, 2016
, 6
, 112950
- Metal-free oxysulfenylation of alkenes with 1-(arylthio)pyrrolidine-2,5-diones and alcohols. Jipan Yu, Chang Gao, Zhixuan Song, Haijun Yang, Hua Fu
, Org. Biomol. Chem.
, 2015
, 13
, 4846
- Iron or boron-catalyzed C–H arylthiation of substituted phenols at room temperature. Hua Tian, Changjin Zhu, Haijun Yang, Hua Fu
, Chem. Commun.
, 2014
, 50
, 8875
- Chiral squaramide-catalysed one-pot enantioselective sulfa-Michael addition/thioesterification of thiols with α,β-unsaturated N-acylated succinimides. Bo-Liang Zhao, Da-Ming Du
, Org. Biomol. Chem.
, 2014
, 12
, 1585