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- Asymmetric organocatalysis: an enabling technology for medicinal chemistry. Bo Han, Xiang-Hong He, Yan-Qing Liu, Gu He, Cheng Peng, Jun-Long Li
, Chem. Soc. Rev.
, 2021
, 50
, 1522
- Enantioselective catalytic Povarov reactions. José Clerigué, M. Teresa Ramos, J. Carlos Menéndez
, Org. Biomol. Chem.
, 2022
, 20
, 1550
- Highly regio- and diastereo-selective synthesis of novel tri- and tetra-cyclic perhydroquinoline architectures via an intramolecular [3 + 2] cycloaddition reaction. M. Bakthadoss, D. Kannan, J. Srinivasan, V. Vinayagam
, Org. Biomol. Chem.
, 2015
, 13
, 2870
- Virtual hydrate screening and coformer selection for improved relative humidity stability. Yuriy A. Abramov
, CrystEngComm
, 2015
, 17
, 5216
- Thiourea as an efficient organocatalyst for the transfer hydrogenation of 2-substituted quinoline derivatives. Xiang Qiao, Zhiguo Zhang, Zongbi Bao, Baogen Su, Huabin Xing, Qiwei Yang, Qilong Ren
, RSC Adv.
, 2014
, 4
, 42566
- Chemodivergent synthesis of functionalized methanodibenzo[b,f][1,5]diazocin-13-ylmethanones and tetrahydroquinolines via solvent-dependent AB2 and A2B2 multicomponent annulation reactions. Isravel Muthukrishnan, Muthu Karuppasamy, B. S. Vachan, Diksha Rajput, Nagarajan Subbiah, C. Uma Maheswari, Vellaisamy Sridharan
, Org. Chem. Front.
, 2020
, 7
, 1616
- Identifying the causative proteins of similar side effect pairs to explore the common molecular basis of these side effects. Yunfeng Wang, Xiujie Chen, Lei Liu, Yuelong Chen, Hongzhe Ma, Ruizhi Yang, Xiangqiong Liu
, Mol. BioSyst.
, 2015
, 11
, 2060
- Prediction of chemical–protein interactions: multitarget-QSAR versus computational chemogenomic methods. Feixiong Cheng, Yadi Zhou, Jie Li, Weihua Li, Guixia Liu, Yun Tang
, Mol. BioSyst.
, 2012
, 8
, 2373
- Heteroatom methods. Jonathan P. Knowles, Andrew Whiting
, Annu. Rep. Prog. Chem., Sect. B: Org. Chem.
, 2010
, 106
, 76
- Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles. Géraldine Masson, Claudia Lalli, Meryem Benohoud, Guillaume Dagousset
, Chem. Soc. Rev.
, 2013
, 42
, 902