Results
1 -
10 of
2042
(Click
here to explore results)
l -Proline, a resolution agent able to target both enantiomers of mandelic acid: an exciting case of stoichiometry controlled chiral resolution . Fuli Zhou, Laurent Collard, Koen Robeyns, Tom Leyssens, Oleksii Shemchuk
, Chem. Commun.
, 2022
, 58
, 8560
Chiral resolution methods for racemic pharmaceuticals based on cocrystal formation . Raha Kaviani, Abolghasem Jouyban, Ali Shayanfar
, CrystEngComm
, 2023
, 25
, 6120
On the pairwise cocrystallization of racemic compounds . Fuli Zhou, Carole Body, Koen Robeyns, Tom Leyssens, Oleksii Shemchuk
, CrystEngComm
, 2023
, 25
, 3060
Enantioselective separation of RS -mandelic acid using β-cyclodextrin modified Fe3 O4 @SiO2 /Au microspheres . Xiaojuan Deng, Wenbin Li, Guosheng Ding, Xiaoping Chen
, Analyst
, 2018
, 143
, 2665
Enantiopure and racemic radical-cation salts of B(mandelate)2
− and B(2-chloromandelate)2
− anions with BEDT-TTF . Toby J. Blundell, Jordan R. Lopez, Kathryn Sneade, John D. Wallis, Hiroki Akutsu, Yasuhiro Nakazawa, Simon J. Coles, Claire Wilson, Lee Martin
, Dalton Trans.
, 2022
, 51
, 4843
A study on the chiral inversion of mandelic acid in humans . Maksims Yevglevskis, Catherine R. Bowskill, Chloe C. Y. Chan, Justin H.-J. Heng, Michael D. Threadgill, Timothy J. Woodman, Matthew D. Lloyd
, Org. Biomol. Chem.
, 2014
, 12
, 6737
The enantiopreference in the solid state probed in lamivudine crystal forms with mandelic acid . Cameron Capeletti da Silva, Felipe Terra Martins
, RSC Adv.
, 2015
, 5
, 20486
Strategies for chiral separation: from racemate to enantiomer . Jingchen Sui, Na Wang, Jingkang Wang, Xin Huang, Ting Wang, Lina Zhou, Hongxun Hao
, Chem. Sci.
, 2023
, 14
, 11955
Ru-catalyzed decarboxylative cyclization of mandelic acids with acrylates: facile access to the phthalide skeleton . Lili Chen, Hongji Li, Feng Yu, Lei Wang
, Chem. Commun.
, 2014
, 50
, 14866
Vanadium(v ) complexes of mandelic acid . Filip Zechel, Peter Schwendt, Róbert Gyepes, Ján Šimunek, Jozef Tatiersky, Lukáš Krivosudský
, New J. Chem.
, 2019
, 43
, 17696