Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
Resolution of trans-1,2-cyclohexanedicarboxylic acid containing two carboxylic groups by forming diastereomeric salts based on feeding molar ratio control
Chirality. 2023 Dec 6. doi: 10.1002/chir.23634. Online ahead of print.ABSTRACTTo investigate the thermodynamic and molecular self-assembly mechanism of trans-1,2-cyclohexane dicarboxylic acid containing two carboxylic acid groups in the chiral resolution process, (S)-phenylethylamine was used as the chiral resolving agent. Two stoichiometric salts were formed when the raw materials were fed at different molar ratios: cyclohexane dicarboxylate monophenylethylamine salt and cyclohexane dicarboxylate diphenylethylamine salt. When the molar ratio of the (S)-phenylethylamine to trans-1,2-cyclohexane dicarboxylic acid was less t...
Source: Chirality - December 7, 2023 Category: Molecular Biology Authors: Xiaoyu Xin Junjie Zhou Quan He Yangfeng Peng Yongming Wei Hongliang Zhao Tianzhong Tong Source Type: research
