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Bond energy enabled amine distinguishing strategy: chemo-, regioselective 1,3-diamination of (trifluoromethyl)alkenes with different amines by two C(sp3 )–F bond cleavages . Hao Zeng, Hengyuan Li, Chengxi Li, Huanfeng Jiang, Chuanle Zhu
, Org. Chem. Front.
, 2022
, 9
, 1383
Original papers in pharmaceutical analysis . G. Carr, A. Islam, P. N. Patsalos, V. D. Goldberg, P. T. Lascelles, P. C. Barrett
, Proc. Anal. Div. Chem. Soc.
, 1975
, 12
, 265
Standardised thin-layer chromatographic systems for the identification of drugs and poisons. A review . A. H. Stead, R. Gill, T. Wright, J. P. Gibbs, A. C. Moffat
, Analyst
, 1982
, 107
, 1106
Solvent-free, uncatalyzed asymmetric “ene” reactions of N-tert -butylsulfinyl-3,3,3-trifluoroacetaldimines: a general approach to enantiomerically pure α-(trifluoromethyl)tryptamines . Giuseppe Mazzeo, Giovanna Longhi, Sergio Abbate, Martina Palomba, Luana Bagnoli, Francesca Marini, Claudio Santi, Jianlin Han, Vadim A. Soloshonok, Emilio Di Crescenzo, Renzo Ruzziconi
, Org. Biomol. Chem.
, 2017
, 15
, 3930
Index pages
, Proc. Anal. Div. Chem. Soc.
, 1975
, 12
, A001
Visible light photocatalysis in the late-stage functionalization of pharmaceutically relevant compounds . Rolando Cannalire, Sveva Pelliccia, Luca Sancineto, Ettore Novellino, Gian Cesare Tron, Mariateresa Giustiniano
, Chem. Soc. Rev.
, 2021
, 50
, 766
Cross-dehydrogenative alkynylation of sulfonamides and amides with terminal alkynes via Ir(iii ) catalysis . Guocai Wu, Wensen Ouyang, Qian Chen, Yanping Huo, Xianwei Li
, Org. Chem. Front.
, 2019
, 6
, 284
Pd-catalysed intramolecular transformations of indolylbenzenesulfonamides: ortho -sulfonamido-bi(hetero)aryls via C2-arylation and polycyclic sultams via C3 arylation . Rajnikanth Sunke, Shabbir Ahmed Khan, K. C. Kumara Swamy
, Org. Biomol. Chem.
, 2022
, 20
, 9148
Novel N -sulfonamide trans -platinum complexes: synthesis, reactivity and in vitro evaluation . José Alemán, Virginia del Solar, Amparo Alvarez-Valdés, Carla Ríos-Luci, José M. Padrón, Carmen Navarro-Ranninger
, Med. Chem. Commun.
, 2011
, 2
, 789
Thiosuccinimide enabled S–N bond formation to access N -sulfenylated sulfonamide derivatives with synthetic diversity . Peifeng Wang, Shan Li, Huiling Wen, Yin Lei, Shujuan Huang, Zixiu Wang, Jialong Su, Wenxiang Guan, Jian Lei
, Org. Biomol. Chem.
, 2024
, 22
, 990