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- Expedient and generic synthesis of imidazole nucleosides by enzymatic transglycosylation. S. Vichier-Guerre, L. Dugué, F. Bonhomme, S. Pochet
, Org. Biomol. Chem.
, 2016
, 14
, 3638
- [4 + 2]Cycloaddition of monocyclic imidazole derivatives with electron-deficient acetylenes. Chiji Yamazaki, Kikumi Katayama, Kieko Suzuki
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 3085
- A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines. Felicia Phei Lin Lim, Lin Yuing Tan, Edward R. T. Tiekink, Anton V. Dolzhenko
, RSC Adv.
, 2018
, 8
, 21495
- Imidazole synthesis by transition metal free, base-mediated deaminative coupling of benzylamines and nitriles. Uttam Kumar Das, Linda J. W. Shimon, David Milstein
, Chem. Commun.
, 2017
, 53
, 13133
- An expedient synthesis of flexible nucleosides via a regiocontrolled enzymatic glycosylation of functionalized imidazoles. S. Vichier-Guerre, L. Dugué, F. Bonhomme, S. Pochet
, Org. Biomol. Chem.
, 2017
, 15
, 8193
- 2′-Deoxyribonucleoside 5′-triphosphates bearing 4-phenyl and 4-pyrimidinyl imidazoles as DNA polymerase substrates. Sophie Vichier-Guerre, Laurence Dugué, Sylvie Pochet
, Org. Biomol. Chem.
, 2019
, 17
, 290
- Direct trifluoromethylation of imidazoheterocycles in a recyclable medium at room temperature. Xiao-Ming Ji, Liang Wei, Fan Chen, Ri-Yuan Tang
, RSC Adv.
, 2015
, 5
, 29766
- A non-linear organic reaction of malonate derivative as a base amplifier to generate imidazoles without producing gas. K. Arimitsu, K. Tomota, S. Fuse, K. Kudo, M. Furutani
, RSC Adv.
, 2016
, 6
, 38388
- Conformational preferences of monohydrated clusters of imidazole derivatives revisited. Aditi Bhattacherjee, Sanjay Wategaonkar
, Phys. Chem. Chem. Phys.
, 2015
, 17
, 20080
- Cost-effective dopant-free star-shaped oligo-aryl amines for high performance perovskite solar cells. Jun-Ying Feng, Kuan-Wen Lai, Yuan-Shin Shiue, Ashutosh Singh, CH. Pavan Kumar, Chun-Ting Li, Wen-Ti Wu, Jiann T. Lin, Chih-Wei Chu, Chien-Cheng Chang, Chao-chin Su
, J. Mater. Chem. A
, 2019
, 7
, 14209