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- A structural spectroscopic study of dissociative anaesthetic methoxphenidine. Bronislav Jurásek, Patrik Fagan, Bohumil Dolenský, Natalie Paškanová, Kristýna Dobšíková, Ivan Raich, Radek Jurok, Vladimír Setnička, Michal Kohout, Jan Čejka, Martin Kuchař
, New J. Chem.
, 2023
, 47
, 4543
- Reversal of the sense of enantioselectivity between 1- and 2-aza[6]helicenes used as chiral inducers of asymmetric autocatalysis. Arimasa Matsumoto, Kento Yonemitsu, Hanae Ozaki, Jiří Míšek, Ivo Starý, Irena G. Stará, Kenso Soai
, Org. Biomol. Chem.
, 2017
, 15
, 1321
- 28. The influence of solvents and of other factors on the rotation of optically active compounds. Part XXXII. The rotation dispersion of esters of dibenzoyl-d-tartaric acid in various solvents. T. S. Patterson, David McCreath
, J. Chem. Soc.
, 1934
, 100
- Chiral recognition of tartaric acid derivatives by a synthetic receptor. Fernando Garcia-Tellado, Jeffrey Albert, Andrew D. Hamilton
, J. Chem. Soc., Chem. Commun.
, 1991
, 1761
- Synthesis of chiral calix[4]arenes bearing aminonaphthol moieties and their use in the enantiomeric recognition of carboxylic acids. Mustafa Durmaz, Mustafa Yilmaz, Abdulkadir Sirit
, Org. Biomol. Chem.
, 2011
, 9
, 571
- Design and synthesis of nanoporous carbon materials using Cd-based homochiral metal–organic frameworks as precursors for supercapacitor application. Guangju Zhang, Siqi Xiu, Ying Wei, Qingguo Zhang, Kedi Cai
, CrystEngComm
, 2018
, 20
, 4364
- New insights into the mechanism of phenolic oxidation with phenyliodonium(III) reagents. László Kürti, Pál Herczegh, Júlia Visy, Miklós Simonyi, Sándor Antus, Andrew Pelter
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 379
- Chiral phosphoric acid catalyzed enantioselective sulfamination of amino-alkenes. Lijun Li, Zequan Li, Deshun Huang, Haining Wang, Yian Shi
, RSC Adv.
, 2013
, 3
, 4523
- Supramolecular host–guest polymeric materials for biomedical applications. Xian Jun Loh
, Mater. Horiz.
, 2014
, 1
, 185
- Chiral supramolecular polymers. Fátima García, Rafael Gómez, Luis Sánchez
, Chem. Soc. Rev.
, 2023
, 52
, 7524