Jordan C, Siebold K, Priegue P, Seeberger P, Gilmour R
J Am Chem Soc. 2024; 146(22):15366-15375.
PMID: 38768956
PMC: 11157539.
DOI: 10.1021/jacs.4c03179.
Fukase K, Manabe Y, Shimoyama A
Front Chem. 2023; 11:1319883.
PMID: 38116104
PMC: 10728286.
DOI: 10.3389/fchem.2023.1319883.
Lin T, Chang J, Wu Y, Sun T, Cheng Y, Ren C
Mol Neurobiol. 2023; 60(7):3873-3882.
PMID: 36976478
DOI: 10.1007/s12035-023-03307-w.
Rohokale R, Guo Z
ACS Infect Dis. 2023; 9(2):178-212.
PMID: 36706246
PMC: 9930202.
DOI: 10.1021/acsinfecdis.2c00559.
Shivatare S, Shivatare V, Wong C
Chem Rev. 2022; 122(20):15603-15671.
PMID: 36174107
PMC: 9674437.
DOI: 10.1021/acs.chemrev.1c01032.
Synthetic Glycans to Improve Current Glycoconjugate Vaccines and Fight Antimicrobial Resistance.
Del Bino L, Osterlid K, Wu D, Nonne F, Romano M, Codee J
Chem Rev. 2022; 122(20):15672-15716.
PMID: 35608633
PMC: 9614730.
DOI: 10.1021/acs.chemrev.2c00021.
Synthetic Carbohydrate Chemistry and Translational Medicine.
Shivatare S, Wong C
J Org Chem. 2020; 85(24):15780-15800.
PMID: 33125238
PMC: 8312278.
DOI: 10.1021/acs.joc.0c01834.
Synthetic carbohydrate-based vaccines: challenges and opportunities.
Mettu R, Chen C, Wu C
J Biomed Sci. 2020; 27(1):9.
PMID: 31900143
PMC: 6941340.
DOI: 10.1186/s12929-019-0591-0.
Oligosaccharide Synthesis and Translational Innovation.
Krasnova L, Wong C
J Am Chem Soc. 2019; 141(9):3735-3754.
PMID: 30716271
PMC: 6538563.
DOI: 10.1021/jacs.8b11005.
Recent Advances in the Synthesis of Glycoconjugates for Vaccine Development.
Colombo C, Pitirollo O, Lay L
Molecules. 2018; 23(7).
PMID: 30011851
PMC: 6099631.
DOI: 10.3390/molecules23071712.
Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges.
Panza M, Pistorio S, Stine K, Demchenko A
Chem Rev. 2018; 118(17):8105-8150.
PMID: 29953217
PMC: 6522228.
DOI: 10.1021/acs.chemrev.8b00051.
Fully Synthetic Self-Adjuvanting α-2,9-Oligosialic Acid Based Conjugate Vaccines against Group C Meningitis.
Liao G, Zhou Z, Suryawanshi S, Mondal M, Guo Z
ACS Cent Sci. 2016; 2(4):210-8.
PMID: 27163051
PMC: 4850515.
DOI: 10.1021/acscentsci.5b00364.
Exploration of the Oxazolidinthione Protecting System for the Synthesis of Sialic Acid Glycosides.
Rajender S, Crich D
J Carbohydr Chem. 2016; 32(5-6):324-335.
PMID: 26807000
PMC: 4723110.
DOI: 10.1080/07328303.2013.804081.
Automated solid-phase synthesis of oligosaccharides containing sialic acids.
Lai C, Hahm H, Liang C, Seeberger P
Beilstein J Org Chem. 2015; 11:617-21.
PMID: 26124863
PMC: 4464161.
DOI: 10.3762/bjoc.11.69.
Synthesis and immunological study of α-2,9-oligosialic acid conjugates as anti-group C meningitis vaccines.
Liao G, Zhou Z, Guo Z
Chem Commun (Camb). 2015; 51(47):9647-50.
PMID: 25973942
PMC: 4526240.
DOI: 10.1039/c5cc01794g.
Chemical synthesis of the repeating unit of type Ia group B Streptococcus capsular polysaccharide.
Mondal P, Liao G, Mondal M, Guo Z
Org Lett. 2015; 17(5):1102-5.
PMID: 25674920
PMC: 4664191.
DOI: 10.1021/ol5036563.
Probing the influence of protecting groups on the anomeric equilibrium in sialic acid glycosides with the persistent radical effect.
Kancharla P, Kato T, Crich D
J Am Chem Soc. 2014; 136(14):5472-80.
PMID: 24606062
PMC: 4004215.
DOI: 10.1021/ja501276r.
Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.
Kancharla P, Crich D
J Am Chem Soc. 2013; 135(50):18999-9007.
PMID: 24261615
PMC: 3917720.
DOI: 10.1021/ja410683y.
Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.
Navuluri C, Crich D
Angew Chem Int Ed Engl. 2013; 52(43):11339-42.
PMID: 24038615
PMC: 3865865.
DOI: 10.1002/anie.201303781.
Dissecting the influence of oxazolidinones and cyclic carbonates in sialic acid chemistry.
Kancharla P, Navuluri C, Crich D
Angew Chem Int Ed Engl. 2012; 51(44):11105-9.
PMID: 22976809
PMC: 3489474.
DOI: 10.1002/anie.201204400.
