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Cyclization of o-phenylenediamines by CO2 in the presence of H2 for the synthesis of benzimidazoles. Bo Yu, Hongye Zhang, Yanfei Zhao, Sha Chen, Jilei Xu, Changliang Huang, Zhimin Liu , Green Chem. , 2013 , 15 , 95

CLXXXIII.—The hydrolysis of diacetyl-o-diamines. Montague Alexandra Phillips , J. Chem. Soc. , 1930 , 1409

CXLIX.—The methylation of benziminazoles. Montague Alexandra Phillips , J. Chem. Soc. , 1931 , 1143

Differential formation of nitrogen-centered radicals leading to unprecedented, regioselective bromination of N,N′-(1,2-phenylene)bisamides and 2-amidophenols. Damoder Reddy Motati, Dilipkumar Uredi, Amarender Goud Burra, J. Phillip Bowen, Frank R. Fronczek, Clint R. Smith, E. Blake Watkins , Org. Chem. Front. , 2020 , 7 , 1095

A novel green route for the synthesis of N-phenylacetamides, benzimidazoles and acridinediones using Candida parapsilosis ATCC 7330. Pula Mahajabeen, Anju Chadha , RSC Adv. , 2013 , 3 , 21972

A live bacteria SERS platform for the in situ monitoring of nitric oxide release from a single MRSA. Zhijun Zhang, Xuemei Han, Zhimin Wang, Zhe Yang, Wenmin Zhang, Juan Li, Huanghao Yang, Xing Yi Ling, Bengang Xing , Chem. Commun. , 2018 , 54 , 7022

Synthesis of amides from acid chlorides and amines in the bio-based solvent Cyrene™. Thomas W. Bousfield, Katharine P. R. Pearce, Simbarashe B. Nyamini, Athanasios Angelis-Dimakis, Jason E. Camp , Green Chem. , 2019 , 21 , 3675

348. Tritylation of ortho-disubstituted benzenes. Systematic differences of activation of ortho- and para-directing groups. Gabriel Chuchani , J. Chem. Soc. , 1959 , 1753

A new kinetic model for the acid-catalysed reactions of N-(2-aminophenyl)phthalamic acid in aqueous media . Christopher J. Perry , J. Chem. Soc., Perkin Trans. 2 , 1997 , 977

XXV.—The formation of 2-methylbenziminazoles. Montague Alexandra Phillips , J. Chem. Soc. , 1928 , 172