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- Ethyl-for-methyl substitution enhances the subtype specificity of mecamylamine analogues. David Mangan, Neasa McNabola, Emily H. Clark, Isabel Bermudez, Susan Wonnacott, J. Mike Southern
, Org. Biomol. Chem.
, 2019
, 17
, 9892
- A new synthesis and preliminary evaluation of some analogues of mecamylamine – a compound with anti-addiction properties. David Mangan, Neasa McNabola, Emily H. Clark, Isabel Bermudez, Susan Wonnacott, J. Mike Southern
, Org. Biomol. Chem.
, 2016
, 14
, 10787
- Unraveling variation on the profile aroma compounds of strong aroma type of Baijiu in different regions by molecular matrix analysis and olfactory analysis. Jiaxin Hong, Junshan Wang, Chunsheng Zhang, Zhigang Zhao, Wenjing Tian, Yashuai Wu, Hao Chen, Dongrui Zhao, Jinyuan Sun
, RSC Adv.
, 2021
, 11
, 33511
- Stereoselective aziridination of cyclic allylic alcohols using chloramine-T. Susannah C. Coote, Peter O'Brien, Adrian C. Whitwood
, Org. Biomol. Chem.
, 2008
, 6
, 4299
- Elucidation of consistent enantioselectivity for a homologous series of chiral compounds in homochiral metal–organic frameworks. Xiaoying Bao, Linda J. Broadbelt, Randall Q. Snurr
, Phys. Chem. Chem. Phys.
, 2010
, 12
, 6466
- Hot water-promoted cyclopropylcarbinyl rearrangement facilitates construction of homoallylic alcohols. Pei-Fang Li, Cheng-Bo Yi, Jin Qu
, Org. Biomol. Chem.
, 2015
, 13
, 5012
- Asymmetric reduction of ketones by Geotrichum candidum in the presence of AmberliteTM XAD, a solid organic solvent. Kaoru Nakamura, Mikio Fujii, Yoshiteru Ida
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 3205
- Enantio- & chemo-selective preparation of enantiomerically enriched aliphatic nitro alcohols using Candida parapsilosis ATCC 7330. Sowmyalakshmi Venkataraman, Anju Chadha
, RSC Adv.
, 2015
, 5
, 73807
- Identification of the maze in the conformational landscape of fenchol. E. M. Neeman, T. R. Huet
, Phys. Chem. Chem. Phys.
, 2018
, 20
, 24708
- Synthesis of substituted norcaranes for use as probes of enzyme mechanisms. Luke R. Churchman, Peter D. Giang, Julia B. Buczynski, Jeanette E. Stok, Stephen G. Bell, James J. De Voss
, Org. Biomol. Chem.
, 2023
, 21
, 9647