Zicheng Li
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Zicheng Li has a total of 41 co-authors. Here are the top co-authors by number of shared publications:
Wencai Huang
Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
6 shared publicationsJiyu Gao
School of Chemical Engineering, Sichuan University, Chengdu, China
4 shared publicationsYan Xiao
Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
4 shared publicationsJianjun Zhou
School of Chemical Engineering, Sichuan University, Chengdu, China
3 shared publicationsTaiping Chen
School of Chemical Engineering, Sichuan University, Chengdu, China
3 shared publicationsYinglan Zhao
State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China
3 shared publications
Latest Publications
- 15 October 2024
- Published by Taylor & Francis in Epigenomics
- Vol. 16 (19-20) , 1301-1313
Dysregulation of epigenetic modifications in inborn errors of immunity
Inborn errors of immunity (IEIs) are a group of typically monogenic disorders characterized by dysfunction in the immune system. Individuals with these disorders experience increased susceptibility to infections, autoimmunity and malignancies due to abnormal immune responses. Epigenetic modifications, including DNA methylation, histone modifications and chromatin remodeling, have been well explored in the regulation of immune cell development and effector function. Aberrant epigenetic modifications can disrupt gene expression profiles crucial for immune responses, resulting in impaired immune cell differentiation and function. Dysregulation of these processes caused by mutations in genes involving in epigenetic modifications has been associated with various IEIs. In this review article, we focus on IEIs that are caused by mutations in 13 genes involved in the regulation of DNA methylation, histone modification and chromatin remodeling.
- 15 October 2024
- Published by Taylor & Francis in Epigenomics
- Vol. 16 (19-20) , 1301-1313
Dysregulation of epigenetic modifications in inborn errors of immunity
Inborn errors of immunity (IEIs) are a group of typically monogenic disorders characterized by dysfunction in the immune system. Individuals with these disorders experience increased susceptibility to infections, autoimmunity and malignancies due to abnormal immune responses. Epigenetic modifications, including DNA methylation, histone modifications and chromatin remodeling, have been well explored in the regulation of immune cell development and effector function. Aberrant epigenetic modifications can disrupt gene expression profiles crucial for immune responses, resulting in impaired immune cell differentiation and function. Dysregulation of these processes caused by mutations in genes involving in epigenetic modifications has been associated with various IEIs. In this review article, we focus on IEIs that are caused by mutations in 13 genes involved in the regulation of DNA methylation, histone modification and chromatin remodeling.
- Open Access
Ionic Liquid Catalyzed Hydrolysis of Sugarcane Cellulose to Produce Reducing Sugar
As the most abundant bioenergy raw material in nature, cellulose can be converted into sugar by hydrolysis, which can be further degraded to produce downstream chemicals, such as polyols. Hydrolysis technology is one of the key steps in the development and utilization of cellulosic biomass resources. In this study, the ionic liquid (IL)-catalyzed hydrolysis of sugarcane cellulose into reducing sugar was studied. Firstly, the hydrolysis of sugarcane cellulose in different ionic liquids (including benzothiazolomethane sulfonate, [HBth][CH3SO3] and 1-methyl-3-(3-sulfopropyl)-imidazolium hydrogen sulfate, [C3SO3Hmim]HSO4) in heterogeneous and homogeneous systems to produce reducing sugar was studied. In a homogeneous system, the catalytic effect of an ionic liquid on sugarcane cellulose was explored. The pretreatment, IL dosage (0.1~1.0 g), reaction temperature (100~180 °C), addition of water (0~500 μL), and time (1~6 h) were all discovered as key conditions for hydrolysis. The acidity of an acidic ionic liquid is a key factor affecting the hydrolysis of sugarcane cellulose; meanwhile, effective pretreatment and water are also important. As a comparison, the catalytic effect of [C3SO3Hmim]HSO4 in heterogeneous systems (the maximum yield of 5.98% for total reducing sugars, TRS) was not as good as that of [HBth][CH3SO3] in homogeneous systems (33.97%). A higher temperature does not necessarily lead to an increased TRS yield, but it will make the maximum TRS appear earlier. At last, 732 cationic ion exchange resin was used to investigate the separation of reducing sugar and ionic liquid, and the recovery of ionic liquid was investigated by an adsorption–desorption experiment. The ionic liquid can be well separated from TRS in the [HBth][CH3SO3] and reused at least five times.
Open AccessIonic Liquid Catalyzed Hydrolysis of Sugarcane Cellulose to Produce Reducing Sugar
As the most abundant bioenergy raw material in nature, cellulose can be converted into sugar by hydrolysis, which can be further degraded to produce downstream chemicals, such as polyols. Hydrolysis technology is one of the key steps in the development and utilization of cellulosic biomass resources. In this study, the ionic liquid (IL)-catalyzed hydrolysis of sugarcane cellulose into reducing sugar was studied. Firstly, the hydrolysis of sugarcane cellulose in different ionic liquids (including benzothiazolomethane sulfonate, [HBth][CH3SO3] and 1-methyl-3-(3-sulfopropyl)-imidazolium hydrogen sulfate, [C3SO3Hmim]HSO4) in heterogeneous and homogeneous systems to produce reducing sugar was studied. In a homogeneous system, the catalytic effect of an ionic liquid on sugarcane cellulose was explored. The pretreatment, IL dosage (0.1~1.0 g), reaction temperature (100~180 °C), addition of water (0~500 μL), and time (1~6 h) were all discovered as key conditions for hydrolysis. The acidity of an acidic ionic liquid is a key factor affecting the hydrolysis of sugarcane cellulose; meanwhile, effective pretreatment and water are also important. As a comparison, the catalytic effect of [C3SO3Hmim]HSO4 in heterogeneous systems (the maximum yield of 5.98% for total reducing sugars, TRS) was not as good as that of [HBth][CH3SO3] in homogeneous systems (33.97%). A higher temperature does not necessarily lead to an increased TRS yield, but it will make the maximum TRS appear earlier. At last, 732 cationic ion exchange resin was used to investigate the separation of reducing sugar and ionic liquid, and the recovery of ionic liquid was investigated by an adsorption–desorption experiment. The ionic liquid can be well separated from TRS in the [HBth][CH3SO3] and reused at least five times.
- 1 January 2024
- Published by Shanghai Institute of Organic Chemistry in Chinese Journal of Organic Chemistry
- Vol. 44 (7) , 2251-2256
Synthesis of 3,5-Diaryl-1,2,4-oxadiazole by One-Pot Homocoupling Reaction
- 1 January 2024
- Published by Shanghai Institute of Organic Chemistry in Chinese Journal of Organic Chemistry
- Vol. 44 (7) , 2251-2256
Synthesis of 3,5-Diaryl-1,2,4-oxadiazole by One-Pot Homocoupling Reaction
- 24 March 2022
- Published by Springer Nature in Monatshefte für Chemie - Chemical Monthly
- Vol. 153 (4) , 359-367
Synthesis and bioactivity evaluation of 5,6-epoxynorcantharidin mono-amide and imide derivatives
- 24 March 2022
- Published by Springer Nature in Monatshefte für Chemie - Chemical Monthly
- Vol. 153 (4) , 359-367
Synthesis and bioactivity evaluation of 5,6-epoxynorcantharidin mono-amide and imide derivatives
- Open Access
- 17 July 2021
- Published by SAGE Publications in Journal of Chemical Research
- Vol. 45 (11-12) , 928-933
Homocoupling of terminal alkynes catalyzed by CuCl under solvent-free conditions
A series of symmetrical 1,4-disubstituted buta-1,3-diynes is prepared with excellent yields (up to 95%) through homocoupling of terminal alkynes catalyzed by a copper salt under solvent-free conditions. This method provides an environmentally friendly process to prepare 1,3-diynes in short reaction times under mild conditions. Furthermore, the method is suitable for a wide substrate scope and has excellent functional group compatibility. The reaction can also be scaled up to gram level.
- 17 July 2021
- Published by SAGE Publications in Journal of Chemical Research
- Vol. 45 (11-12) , 928-933
Open AccessHomocoupling of terminal alkynes catalyzed by CuCl under solvent-free conditions
A series of symmetrical 1,4-disubstituted buta-1,3-diynes is prepared with excellent yields (up to 95%) through homocoupling of terminal alkynes catalyzed by a copper salt under solvent-free conditions. This method provides an environmentally friendly process to prepare 1,3-diynes in short reaction times under mild conditions. Furthermore, the method is suitable for a wide substrate scope and has excellent functional group compatibility. The reaction can also be scaled up to gram level.
- 17 April 2021
- Published by Springer Nature in Monatshefte für Chemie - Chemical Monthly
- Vol. 152 (5) , 545-549
Synthesis of hydroxy-γ-sanshool
- 17 April 2021
- Published by Springer Nature in Monatshefte für Chemie - Chemical Monthly
- Vol. 152 (5) , 545-549
Synthesis of hydroxy-γ-sanshool
- Open Access
- 26 November 2020
- Published by SAGE Publications in Journal of Chemical Research
- Vol. 45 (3-4) , 310-314
Synthesis of hydroxy-α-sanshool
Hydroxy-α-sanshool was synthesized in a 13% overall yield through eight steps, which included two Wittig reactions that were used to form the carbon skeleton with ethyl 2-oxoacetate and 2 E,4 E-hexadienal being reacted with the appropriate ylides. Impurities in the processes could easily be separated. Ethyl 6-hydroxy-2Z-hexenoate was converted to its E-isomer with catalysis by I2 and 2E,6Z,8E,10E-dodecatetraenoic acid was crystallized from a solution in 1% ethyl acetate in n-hexane.
- 26 November 2020
- Published by SAGE Publications in Journal of Chemical Research
- Vol. 45 (3-4) , 310-314
Open AccessSynthesis of hydroxy-α-sanshool
Hydroxy-α-sanshool was synthesized in a 13% overall yield through eight steps, which included two Wittig reactions that were used to form the carbon skeleton with ethyl 2-oxoacetate and 2 E,4 E-hexadienal being reacted with the appropriate ylides. Impurities in the processes could easily be separated. Ethyl 6-hydroxy-2Z-hexenoate was converted to its E-isomer with catalysis by I2 and 2E,6Z,8E,10E-dodecatetraenoic acid was crystallized from a solution in 1% ethyl acetate in n-hexane.
- 24 May 2020
- Published by Springer Nature in Chemical Papers
- Vol. 74 (11) , 3873-3886
Synthesis and biological evaluation of innovative thiourea derivatives as PHGDH inhibitors
- 24 May 2020
- Published by Springer Nature in Chemical Papers
- Vol. 74 (11) , 3873-3886
Synthesis and biological evaluation of innovative thiourea derivatives as PHGDH inhibitors
- 5 June 2019
- Published by Springer Nature in Chemical Papers
- Vol. 73 (11) , 2813-2820
Synthesis and characterization of furazan derivatives and their evaluation as antitumor agents
- 5 June 2019
- Published by Springer Nature in Chemical Papers
- Vol. 73 (11) , 2813-2820
Synthesis and characterization of furazan derivatives and their evaluation as antitumor agents
- 14 March 2014
- Published by Springer Nature in Medicinal Chemistry Research
- Vol. 23 (9) , 4050-4059
Synthesis and evaluation of 2-(2-((4-substituted-phenoxy)methyl)-1H-benzo[d] imidazol-1-yl)acetohydrazone derivatives as antitumor agents
- 14 March 2014
- Published by Springer Nature in Medicinal Chemistry Research
- Vol. 23 (9) , 4050-4059
Synthesis and evaluation of 2-(2-((4-substituted-phenoxy)methyl)-1H-benzo[d] imidazol-1-yl)acetohydrazone derivatives as antitumor agents