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- A facile manganese dioxide mediated oxidation of primary benzylamines to benzamides. A. Poeschl, D. M. Mountford
, Org. Biomol. Chem.
, 2014
, 12
, 7150
- Cultivation of a Cu/HMPC catalyst from a hyperaccumulating mustard plant for highly efficient and selective coupling reactions under mild conditions. Mayakrishnan Gopiraman, Kai Wei, Ke-Qin Zhang, Ill-Min Chung, Ick Soo Kim
, RSC Adv.
, 2018
, 8
, 4531
- A new model of binding of rifampicin and its amino analogues as zwitterions to bacterial RNA polymerase. Krystian Pyta, Piotr Przybylski, Katarzyna Klich, Joanna Stefańska
, Org. Biomol. Chem.
, 2012
, 10
, 8283
- Halogen bonding for the design of inhibitors by targeting the S1 pocket of serine proteases. Longguang Jiang, Xu Zhang, Yang Zhou, Yayu Chen, Zhipu Luo, Jinyu Li, Cai Yuan, Mingdong Huang
, RSC Adv.
, 2018
, 8
, 28189
- Index of subjects, 1946
, J. Chem. Soc.
, 1946
, 1184
- Influence of the organic linker substituent on the catalytic activity of MIL-101(Cr) for the oxidative coupling of benzylamines to imines. Andrea Santiago-Portillo, Juan F. Blandez, Sergio Navalón, Mercedes Álvaro, Hermenegildo García
, Catal. Sci. Technol.
, 2017
, 7
, 1351
- Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base. Zhao Li, Carol Gelbaum, Zachary S. Campbell, Paul C. Gould, Jason S. Fisk, Bruce Holden, Arvind Jaganathan, Gregory T. Whiteker, Pamela Pollet, Charles L. Liotta
, New J. Chem.
, 2017
, 41
, 15420
- Conjugated HCl-doped polyaniline for photocatalytic oxidative coupling of amines under visible light. Peng Kong, Pei Liu, Zhenyu Ge, Hao Tan, Linjuan Pei, Jie Wang, Pengqi Zhu, Xianmo Gu, Zhanfeng Zheng, Zhong Li
, Catal. Sci. Technol.
, 2019
, 9
, 753
- Cobalt catalysed aminocarbonylation of thiols in batch and flow for the preparation of amides. Jose Maria Orduña, Gema Domínguez, Javier Pérez-Castells
, RSC Adv.
, 2021
, 11
, 30398
- Convenient and clean synthesis of imines from primary benzylamines. Guobiao Chu, Chunbao Li
, Org. Biomol. Chem.
, 2010
, 8
, 4716