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- Use of molecular electrostatic potential for quantitative assessment of inductive effect. Cherumuttathu H. Suresh, P. Alexander, K. Periya Vijayalakshmi, P. K. Sajith, Shridhar R. Gadre
, Phys. Chem. Chem. Phys.
, 2008
, 10
, 6492
- Photoinduced, metal- and photosensitizer-free decarboxylative C–H (amino)alkylation of heteroarenes in a sustainable solvent. Jun Xu, Chenfeng Liang, Jiabin Shen, Qing Chen, Wanmei Li, Pengfei Zhang
, Green Chem.
, 2023
, 25
, 1975
- Ring effect on helical twisting power of optically active mesogenic esters derived from benzene, bicyclo[2.2.2]octane and p-carborane carboxylic acids. Adam Januszko, Piotr Kaszynski, Witold Drzewinski
, J. Mater. Chem.
, 2006
, 16
, 452
- Convenient synthesis of 6-alkyl phenanthridines and 1-alkyl isoquinolines via silver-catalyzed oxidative radical decarboxylation. Qian Yao, Xin Zhou, Xiuli Zhang, Cong Wang, Peng Wang, Ming Li
, Org. Biomol. Chem.
, 2017
, 15
, 957
- Quantum topological molecular similarity. Part 5. Further development with an application to the toxicity of polychlorinated dibenzo-p-dioxins(PCDDs). P. L. A. Popelier, U. A. Chaudry, P. J. Smith
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 1231
- Metal-free photosensitized aminosulfonylation of alkenes: a practical approach to β-amido sulfones. Meiling Chen, Wenyan Sun, Jingjing Yang, LuLu Yuan, Jian-Qiang Chen, Jie Wu
, Green Chem.
, 2023
, 25
, 3857
- Introducing DDEC6 atomic population analysis: part 2. Computed results for a wide range of periodic and nonperiodic materials. Nidia Gabaldon Limas, Thomas A. Manz
, RSC Adv.
, 2016
, 6
, 45727
- Facile solvolysis of a surprisingly twisted tertiary amide. Aaron J. Bloomfield, Subhajyoti Chaudhuri, Brandon Q. Mercado, Victor S. Batista, Robert H. Crabtree
, New J. Chem.
, 2016
, 40
, 1974
- CNDO/2 Molecular orbital calculations and the existence of an electric field effect upon proton chemical shifts. G. K. Hamer, W. F. Reynolds
, J. Chem. Soc. D
, 1971
, 1218
- Steric effects of polar substituents evaluated in terms of energy by means of isodesmic reactions. Stanislav Böhm, Otto Exner
, Org. Biomol. Chem.
, 2008
, 6
, 1092