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Regioselective deoxygenative chalcogenation of 7-azindole N-oxides promoted by I2/PEG-200. Shanshan Liu, Heng Yang, Lin-Yu Jiao, Jian-Hua Zhang, Chen Zhao, Yangmin Ma, Xiufang Yang , Org. Biomol. Chem. , 2019 , 17 , 10073

Structure-based de novo design and identification of D816V mutant-selective c-KIT inhibitors. Hwangseo Park, Soyoung Lee, Suhyun Lee, Sungwoo Hong , Org. Biomol. Chem. , 2014 , 12 , 4644

Rhodium(iii)-catalyzed C–C coupling of 7-azaindoles with vinyl acetates and allyl acetates. Shuai-Shuai Li, Cheng-Qi Wang, Hui Lin, Xiao-Mei Zhang, Lin Dong , Org. Biomol. Chem. , 2016 , 14 , 229

Syntheses and properties of 1H-pyrrolo[2,3-b]pyridines. R. Herbert, D. G. Wibberley , J. Chem. Soc. C , 1969 , 1505

Regioselective Ir(iii)-catalyzed C–H alkynylation directed by 7-azaindoles. Bin Liu, Xin Wang, Zemei Ge, Runtao Li , Org. Biomol. Chem. , 2016 , 14 , 2944

Facile synthesis of 4- and 7-azaindoles from the corresponding imines by palladium-catalyzed cascade C–C and C–N coupling. Ngo Nghia Pham, Thanh Tuan Dang, Ngoc Thang Ngo, Alexander Villinger, Peter Ehlers, Peter Langer , Org. Biomol. Chem. , 2015 , 13 , 6047

Rh(iii)-catalyzed C–H oxidative ortho-olefination of arenes using 7-azaindole as a directing group and utilization in the construction of new tetracyclic heterocycles containing a 7-azaindole skeleton. Bin Liu, Ridong Li, Wei Zhan, Xin Wang, Zemei Ge, Runtao Li , RSC Adv. , 2016 , 6 , 48205

1H-pyrrolo[2,3-b]pyridines. Part II. Fragmentation of some 1H-pyrrolo[2,3-b]pyridines induced by electron impact. R. Herbert, D. G. Wibberley , J. Chem. Soc. B , 1970 , 459

The acid-catalysed synthesis of 7-azaindoles from 3-alkynyl-2-aminopyridines and their antimicrobial activity. Tlabo C. Leboho, Sandy F. van Vuuren, Joseph P. Michael, Charles B. de Koning , Org. Biomol. Chem. , 2014 , 12 , 307

De novo design, synthesis and pharmacological evaluation of new azaindole derivatives as dual inhibitors of Abl and Src kinases. Gwénaël Chevé, Cédric Bories, Bénédicte Fauvel, François Picot, Alix Tible, Bénédicte Daydé-Cazals, Olivier Loget, Aziz Yasri , Med. Chem. Commun. , 2012 , 3 , 788