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- Aza-Claisen rearrangement of 2-C-hydroxymethyl glycals as a versatile strategy towards synthesis of isofagomine and related biologically important azasugars. Y. Suman Reddy, Pavan K. Kancharla, Rashmi Roy, Yashwant D. Vankar
, Org. Biomol. Chem.
, 2012
, 10
, 2760
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Base-catalyzed reactions of environmentally relevant N-chloro-piperidines. A quantum-chemical study. Davor Šakić, Hendrik Zipse, Valerije Vrček
, Org. Biomol. Chem.
, 2011
, 9
, 4336
- The chemical fate of paroxetine
metabolites. Dehydration of radicals derived from 4-(4-fluorophenyl)-3-(hydroxymethyl)piperidine. Davor Šakić, Florian Achrainer, Valerije Vrček, Hendrik Zipse
, Org. Biomol. Chem.
, 2013
, 11
, 4232
- Synthesis and evaluation of amide, sulfonamide and urea – benzisoxazole derivatives as potential atypical antipsychotics. Yin Chen, Yu Lan, Xudong Cao, Xiangqing Xu, Juecheng Zhang, Minquan Yu, Xin Liu, Bi-Feng Liu, Guisen Zhang
, Med. Chem. Commun.
, 2015
, 6
, 831
- Integrated CO2 capture and electrochemical upgradation: the underpinning mechanism and techno-chemical analysis. Sandip Kumar De, Dong-Il Won, Jeongwon Kim, Dong Ha Kim
, Chem. Soc. Rev.
, 2023
, 52
, 5744
- Peperomin E and its synthetic amino derivatives: potent agents targeting leukaemia stem cells. Ming Gao, Xin-zhi Wang, Ye-ting Shu, Jie Liang, Liang Chen, Rui Liu, Jing-yu Liang, Hong-mei Wen
, RSC Adv.
, 2017
, 7
, 52200
- Synthesis of polyhydroxy piperidines and their analogues: a novel approach towards selective inhibitors of α-glucosidase. Ganesh Pandey, Kishor Chandra Bharadwaj, M. Islam Khan, K. S. Shashidhara, Vedavati G. Puranik
, Org. Biomol. Chem.
, 2008
, 6
, 2587
- A new access to polyhydroxy piperidines of the azasugar class: synthesis and glycosidase inhibition studies. Ganesh Pandey, Manmohan Kapur, M. Islam Khan, Sushama M. Gaikwad
, Org. Biomol. Chem.
, 2003
, 1
, 3321
- The influence of the stereochemistry of the nitrogen centre on proton chemical shifts and on 1H–1H and 15N–1H spin–spin coupling in tetrahydro-1,3-oxazines. F. G. Riddell, J. M. Lehn
, J. Chem. Soc. B
, 1968
, 1224