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Efficient selective synthesis of 2-substituted indoles from complex-base-promoted arynic cyclisations . Catherine Kuehm-Caubère, Ivan Rodriguez, Bruno Pfeiffer, Pierre Renard, Paul Caubère
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2857
Rose bengal as photocatalyst: visible light-mediated Friedel–Crafts alkylation of indoles with nitroalkenes in water . Zong-Yi Yu, Jing-Nan Zhao, Fan Yang, Xiao-Fei Tang, Yu-Feng Wu, Cun-Fei Ma, Bo Song, Lei Yun, Qing-Wei Meng
, RSC Adv.
, 2020
, 10
, 4825
I2 -Triggered N–O cleavage of ketoxime acetates for the synthesis of 3-(4-pyridyl)indoles . Qinghe Gao, Yakun Wang, Qianqian Wang, Yanping Zhu, Zhaomin Liu, Jixia Zhang
, Org. Biomol. Chem.
, 2018
, 16
, 9030
Trifluoromethylselenolation and N -acylation of indoles with [Me4 N][SeCF3 ] . Kai-Li Tan, Hao-Nan Wang, Tao Dong, Cheng-Pan Zhang
, Org. Biomol. Chem.
, 2021
, 19
, 5368
Tandem catalytic oxidative deacetylation of acetoacetic esters and heteroaromatic cyclizations . Yeming Ju, Di Miao, Ruiyang Yu, Sangho Koo
, Org. Biomol. Chem.
, 2015
, 13
, 2588
In(OTf)3 catalyzed C3-benzylation of indoles with benzyl alcohols in water . Lin Wu, Ran Jiang, Jin-Ming Yang, Shun-Yi Wang, Shun-Jun Ji
, RSC Adv.
, 2013
, 3
, 5459
Efficient ZnBr2 -catalyzed reactions of allylic alcohols with indoles , sulfamides and anilines under high-speed vibration milling conditions . Guang-Peng Fan, Zi Liu, Guan-Wu Wang
, Green Chem.
, 2013
, 15
, 1659
Organocatalytic enantioselective Friedel–Crafts reaction: an efficient access to chiral isoindolo-β-carboline derivatives . Fang Fang, Genghong Hua, Feng Shi, Pengfei Li
, Org. Biomol. Chem.
, 2015
, 13
, 4395
Silver-catalyzed TEMPO oxidative homocoupling of indoles for the synthesis of 3,3′-biindolin-2-ones . Feng Lin, Yu Chen, Baoshuang Wang, Wenbing Qin, Liangxian Liu
, RSC Adv.
, 2015
, 5
, 37018
Indoles
via Knoevenagel–Hemetsberger reaction sequence . William L. Heaner IV, Carol S. Gelbaum, Leslie Gelbaum, Pamela Pollet, Kent W. Richman, William DuBay, Jeffrey D. Butler, Gregory Wells, Charles L. Liotta
, RSC Adv.
, 2013
, 3
, 13232