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- Inhibitory selectivity to the AKR1B10 and aldose reductase (AR): insight from molecular dynamics simulations and free energy calculations. Ping Lin, Yuzhen Niu
, RSC Adv.
, 2023
, 13
, 26709
- End-point determination on-line and reaction co-ordinate modelling of homogeneous and heterogeneous reactions in principal component space using periodic near-infrared monitoring. Timothy Norris, Paul K. Aldridge
, Analyst
, 1996
, 121
, 1003
- Benzodiazines: recent synthetic advances. Thomas Mathew, Attila Á. Papp, Farzaneh Paknia, Santos Fustero, G. K. Surya Prakash
, Chem. Soc. Rev.
, 2017
, 46
, 3060
- A ball-milling strategy for the synthesis of benzothiazole, benzimidazole and benzoxazole derivatives under solvent-free conditions. Hemant Sharma, Narinder Singh, Doo Ok Jang
, Green Chem.
, 2014
, 16
, 4922
- Controllable assembly of the benzothiazole framework using a CC triple bond as a one-carbon synthon. Yubing Huang, Donghao Yan, Xu Wang, Peiqi Zhou, Wanqing Wu, Huanfeng Jiang
, Chem. Commun.
, 2018
, 54
, 1742
- Copper-catalyzed synthesis of benzazoles via aerobic oxidative condensation of o-amino/mercaptan/hydroxyanilines with benzylamines. Tiebo Xiao, Shengwei Xiong, Yang Xie, Xichang Dong, Lei Zhou
, RSC Adv.
, 2013
, 3
, 15592
- An efficient synthesis of benzothiazole using tetrabromomethane as a halogen bond donor catalyst. Imran Kazi, Govindasamy Sekar
, Org. Biomol. Chem.
, 2019
, 17
, 9743
- Amberlite IR-120(H)-mediated “on water” synthesis of novel anticancer ruthenium(ii)–p-cymene 2-pyridinylbenzothiazole (BTZ), 2-pyridinylbenzoxazole (BOZ) & 2-pyridinylbenzimidazole (BIZ) scaffolds. Sunisha Kottukulam Subran, Swagata Banerjee, Ashaparna Mondal, Priyankar Paira
, New J. Chem.
, 2016
, 40
, 10333
- Piperazinylpyrimidine modified MCM-41 for the ecofriendly synthesis of benzothiazoles by the simple cleavage of disulfide in the presence of molecular O2. Suman Ray, Paramita Das, Biplab Banerjee, Asim Bhaumik, Chhanda Mukhopadhyay
, RSC Adv.
, 2015
, 5
, 72745
- Iron catalyzed efficient synthesis of 2-arylbenzothiazoles from benzothiazole and olefins using environmentally benign molecular oxygen as oxidant. Ashok B. Khemnar, Bhalchandra M. Bhanage
, RSC Adv.
, 2014
, 4
, 8939