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Publikationer som ChEBI hänvisar till för D-tartaric acid. Visa hela publikationsregistret

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Publications in the selection

10 hits

Bibliografisk träff 2024-08-22

Improved photostability, solubility, hygroscopic stability and antimicrobial activity of fleroxacin by synthesis of fleroxacin-D-tartaric acid pharmaceutical salt.

Liu L, Wang Y, Sun J, Zhang Y, Zhang X, Wu L, Liu Y, Zhang X, Xia Y, Zhang Q, Gao N.

Eur J Pharm Biopharm · journal article · DOI 10.1016/j.ejpb.2024.114464

Bibliografisk träff 2024-08-06

Atomic-scale origin of the enantiospecific decomposition of tartaric acid on chiral copper surfaces.

Daniels AS, Gellman AJ, Sykes ECH.

Chem Commun (Camb) · journal article · DOI 10.1039/d4cc02384f

Bibliografisk träff 2024-06-08

An enantioselective formal synthesis of thienamycin.

Breunig JL, Lin YC, Pierce JG.

Tetrahedron Lett · research-article; journal article · DOI 10.1016/j.tetlet.2024.155132

Bibliografisk träff 2023-12-18

Calcium l-Malate and d-Tartarate Frameworks as Adjuvants for the Sustainable Delivery of a Fungicide.

Ahmad Aljafree NF, Ahmad MF, Abd Aziz U, Borzehandani MY, Mohamad Jaafar A, Asib N, Nguyen HL, Mohamed Tahir MI, Mohammad Latif MA, Cordova KE, Abdul Rahman MB.

ACS Appl Mater Interfaces · journal article · DOI 10.1021/acsami.3c11697

Bibliografisk träff 2023-06-27

D-tartaric acid doping improves the performance of whole-cell bacteria imprinted polymer for sensing Vibrio parahaemolyticus.

Jia X, Liu J, Zhang Y, Jiang X, Zhang J, Wu J.

Anal Chim Acta · journal article · DOI 10.1016/j.aca.2023.341567

Bibliografisk träff 2023-06-12

Effect of Boric Acid on the Ionization Equilibrium of α-Hydroxy Carboxylic Acids and the Study of Its Applications.

Qin R, Chen H, Wen R, Li G, Meng Z.

Molecules · research-article; journal article · DOI 10.3390/molecules28124723

Bibliografisk träff 2023-04-17

Chiral-Controlled Cyclic Chemiluminescence Reactions for the Analysis of Enantiomer Amino Acids.

Zhong Y, Chen Y, Chen L, Hu Y, Xiao X, Xia L, Li G.

Anal Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/acs.analchem.3c00362

Bibliografisk träff 2022-10-05

Impact of Weissella cibaria BYL4.2 and its supernatants on Penicillium chrysogenum metabolism.

Yao D, Wang X, Ma L, Wu M, Xu L, Yu Q, Zhang L, Zheng X.

Front Microbiol · research-article; journal article · DOI 10.3389/fmicb.2022.983613

Bibliografisk träff 2022-10-05

Computer-Based Identification of Potential Druggable Targets in Multidrug-Resistant Acinetobacter baumannii: A Combined In Silico, In Vitro and In Vivo Study.

Badie OH, Basyony AF, Samir R.

Microorganisms · research-article; journal article · DOI 10.3390/microorganisms10101973

Bibliografisk träff 2021-08-18

Subtle Modification of Imine-linked Helical Receptors to Significantly Alter their Binding Affinities and Selectivities for Chiral Guests.

Song G, Kim KM, Lee S, Jeong KS.

Chem Asian J · journal article · DOI 10.1002/asia.202100768

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Publications in the selection

Improved photostability, solubility, hygroscopic stability and antimicrobial activity of fleroxacin by synthesis of fleroxacin-D-tartaric acid pharmaceutical salt.

Atomic-scale origin of the enantiospecific decomposition of tartaric acid on chiral copper surfaces.

An enantioselective formal synthesis of thienamycin.

Calcium l-Malate and d-Tartarate Frameworks as Adjuvants for the Sustainable Delivery of a Fungicide.

D-tartaric acid doping improves the performance of whole-cell bacteria imprinted polymer for sensing Vibrio parahaemolyticus.

Effect of Boric Acid on the Ionization Equilibrium of α-Hydroxy Carboxylic Acids and the Study of Its Applications.

Chiral-Controlled Cyclic Chemiluminescence Reactions for the Analysis of Enantiomer Amino Acids.

Impact of <i>Weissella cibaria</i> BYL4.2 and its supernatants on <i>Penicillium chrysogenum</i> metabolism.

Computer-Based Identification of Potential Druggable Targets in Multidrug-Resistant <i>Acinetobacter baumannii</i>: A Combined In Silico, In Vitro and In Vivo Study.

Subtle Modification of Imine-linked Helical Receptors to Significantly Alter their Binding Affinities and Selectivities for Chiral Guests.