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- Reframing primary alkyl amines as aliphatic building blocks. Kathleen J. Berger, Mark D. Levin
, Org. Biomol. Chem.
, 2021
, 19
, 11
- 1191. The reaction of primary amines with boron halides. Part I. Alkylamines: the preparation of borazoles and borazocines. H. S. Turner, R. J. Warne
, J. Chem. Soc.
, 1965
, 6421
- Native functional group directed distal C(sp3)–H activation of aliphatic systems. Saghnik Saha, Jayabrata Das, Shaeel Ahmed Al-Thabaiti, Soha M. Albukhari, Qana A. Alsulami, Debabrata Maiti
, Catal. Sci. Technol.
, 2023
, 13
, 11
- Recent advances in chelation-assisted site- and stereoselective alkenyl C–H functionalization. Jian Zhang, Xiunan Lu, Cong Shen, Liangyao Xu, Liyuan Ding, Guofu Zhong
, Chem. Soc. Rev.
, 2021
, 50
, 3263
- 913. Metal ions and complexes in organic reactions. Part V. Oxidations of primary and secondary amines with argentic picolinate. R. G. R. Bacon, W. J. W. Hanna
, J. Chem. Soc.
, 1965
, 4962
- ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes. Md. Mahbubur Rahman, Guangrong Meng, Elwira Bisz, Błażej Dziuk, Roger Lalancette, Roman Szostak, Michal Szostak
, Chem. Sci.
, 2023
, 14
, 5141
- Structure–activity relationships in Toll-like receptor 7 agonistic 1H-imidazo[4,5-c]pyridines. Euna Yoo, Breanna M. Crall, Rajalakshmi Balakrishna, Subbalakshmi S. Malladi, Lauren M. Fox, Alec R. Hermanson, Sunil A. David
, Org. Biomol. Chem.
, 2013
, 11
, 6526
- Advances in the development of catalytic tethering directing groups for C–H functionalization reactions. Huan Sun, Nicolas Guimond, Yong Huang
, Org. Biomol. Chem.
, 2016
, 14
, 8389
- Phospholipophilicity of C
x
H
y
N+ amines: chromatographic descriptors and molecular simulations for understanding partitioning into membranes. S. T. J. Droge, J. L. M. Hermens, J. Rabone, S. Gutsell, G. Hodges
, Environ. Sci.: Processes Impacts
, 2016
, 18
, 1011
- Using membrane–water partition coefficients in a critical membrane burden approach to aid the identification of neutral and ionizable chemicals that induce acute toxicity below narcosis levels. Steven T. J. Droge, Geoff Hodges, Mark Bonnell, Steve Gutsell, Jayne Roberts, Alexandre Teixeira, Elin L. Barrett
, Environ. Sci.: Processes Impacts
, 2023
, 25
, 621