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Silver catalyzed intramolecular cyclization for synthesis of 3-alkylideneoxindoles via C–H functionalization. Hong-Li Wang, Zhe Li, Gang-Wei Wang, Shang-Dong Yang
, Chem. Commun.
, 2011
, 47
, 11336
- Diastereoselective synthesis of spiro[benzo[d]pyrrolo[2,1-b]thiazole-3,3′-indolines] via cycloaddition reaction of N-phenacylbenzothiazolium bromides and 3-methyleneoxindoles. Guo-Liang Shen, Jing Sun, Chao-Guo Yan
, Org. Biomol. Chem.
, 2015
, 13
, 10929
- DDQ dehydrogenative Diels–Alder reaction for the synthesis of functionalized spiro[carbazole-1,3′-indolines] and spiro[carbazole-1,5′-pyrimidines]. Shao-Cong Zhan, Ren-Jie Fang, Ren-Yin Yang, Ru-Fang Zhao, Yang Wang, Jing Sun, Chao-Guo Yan
, New J. Chem.
, 2021
, 45
, 15423
- Molecular diversity of the cyclization reaction of 3-methyleneoxindoles with 2-(3,4-dihydronaphthalen-1(2H)-ylidene)malononitriles. Yu-Ling Lu, Jing Sun, Ya-Jing Xie, Chao-Guo Yan
, RSC Adv.
, 2016
, 6
, 23390
- A [3+2] cycloaddition reaction for the synthesis of spiro[indoline-3,3′-pyrrolidines] and evaluation of cytotoxicity towards cancer cells. Ying Huang, Yi-Xin Huang, Jing Sun, Chao-Guo Yan
, New J. Chem.
, 2019
, 43
, 8903
- Molecular diversity of TEMPO-mediated cycloaddition of ketohydrazones and 3-phenacylideneoxindoles. Rong Ye, Jing Sun, Ying Han, Chao-Guo Yan
, New J. Chem.
, 2021
, 45
, 5075
- Convenient synthesis of functionalized spiro[indoline-3,2′-pyrrolizines] or spiro[indoline-3,3′-pyrrolidines] via multicomponent reactions. Jing Sun, Liang Chen, Hui Gong, Chao-Guo Yan
, Org. Biomol. Chem.
, 2015
, 13
, 5905
- Diastereoselective construction of carbazole-based spirooxindoles via the Levy three-component reaction. Shao-Cong Zhan, Jing Sun, Ru-Zhang Liu, Chao-Guo Yan
, Org. Biomol. Chem.
, 2020
, 18
, 163
- Application of the aza-Diels–Alder reaction in the synthesis of natural products. Min-Hui Cao, Nicholas J. Green, Sheng-Zhen Xu
, Org. Biomol. Chem.
, 2017
, 15
, 3105
- Novel synthesis of oxindoles from carbamoyl
chlorides via palladium catalysed cyclisation–anion
capture. Mark R. Fielding, Ronald Grigg, Christopher J. Urch
, Chem. Commun.
, 2000
, 2239