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For: Crich D. En Route to the Transformation of Glycoscience: A Chemist's Perspective on Internal and External Crossroads in Glycochemistry. J Am Chem Soc 2021;143:17-34. [PMID: 33350830 DOI: 10.1021/jacs.0c11106] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Li KJ, Bennett CS. New chemical processes to streamline carbohydrate synthesis. Curr Opin Chem Biol 2022;70:102184. [PMID: 35863085 DOI: 10.1016/j.cbpa.2022.102184] [Reference Citation Analysis]
2 Singh Y, Geringer SA, Demchenko AV. Synthesis and Glycosidation of Anomeric Halides: Evolution from Early Studies to Modern Methods of the 21st Century. Chem Rev 2022;122:11701-58. [PMID: 35675037 DOI: 10.1021/acs.chemrev.2c00029] [Reference Citation Analysis]
3 Pertel SS, Seryi SA, Kakayan ES, Zinin AI, Kononov LO. New methods for the synthesis of 2-(2,2,2-trichloroethoxy)-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyrano)-[2,1-d]-2-oxazoline and its use for stereo-, chemo- and regioselective glycosylation. Carbohydr Res 2022;520:108633. [PMID: 35868150 DOI: 10.1016/j.carres.2022.108633] [Reference Citation Analysis]
4 Zhang Y, Hu Y, Liu S, He H, Sun R, Lu G, Xiao G. Total synthesis of Lentinus giganteus glycans with antitumor activities via stereoselective α-glycosylation and orthogonal one-pot glycosylation strategies. Chem Sci 2022;13:7755-64. [PMID: 35865907 DOI: 10.1039/d2sc02176e] [Reference Citation Analysis]
5 Remmerswaal WA, Houthuijs KJ, van de Ven R, Elferink H, Hansen T, Berden G, Overkleeft HS, van der Marel GA, Rutjes FPJT, Filippov DV, Boltje TJ, Martens J, Oomens J, Codée JDC. Stabilization of Glucosyl Dioxolenium Ions by "Dual Participation" of the 2,2-Dimethyl-2-(ortho-nitrophenyl)acetyl (DMNPA) Protection Group for 1,2-cis-Glucosylation. J Org Chem 2022. [PMID: 35748115 DOI: 10.1021/acs.joc.2c00808] [Reference Citation Analysis]
6 Mukherjee MM, Ghosh R, Hanover JA. Recent Advances in Stereoselective Chemical O-Glycosylation Reactions. Front Mol Biosci 2022;9:896187. [DOI: 10.3389/fmolb.2022.896187] [Reference Citation Analysis]
7 Braak FT, Elferink H, Houthuijs KJ, Oomens J, Martens J, Boltje TJ. Characterization of Elusive Reaction Intermediates Using Infrared Ion Spectroscopy: Application to the Experimental Characterization of Glycosyl Cations. Acc Chem Res 2022. [PMID: 35616920 DOI: 10.1021/acs.accounts.2c00040] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Liu X, Song Y, Liu A, Zhou Y, Zhu Q, Lin Y, Sun H, Zhu K, Liu W, Ding N, Xie W, Sun H, Yu B, Xu P, Li W. More than a Leaving Group: N-Phenyltrifluoroacetimidate as a Remote Directing Group for Highly α-Selective 1,2-cis Glycosylation. Angew Chem Int Ed Engl 2022;61:e202201510. [PMID: 35266604 DOI: 10.1002/anie.202201510] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Cao X, Du X, Jiao H, An Q, Chen R, Fang P, Wang J, Yu B. Carbohydrate-based drugs launched during 2000−2021. Acta Pharmaceutica Sinica B 2022. [DOI: 10.1016/j.apsb.2022.05.020] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Zhang C, Zuo H, Lee GY, Zou Y, Dang Q, Houk KN, Niu D. Halogen-bond-assisted radical activation of glycosyl donors enables mild and stereoconvergent 1,2-cis-glycosylation. Nat Chem . [DOI: 10.1038/s41557-022-00918-z] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
11 Zhao WC, Li RP, Ma C, Liao QY, Wang M, He ZT. Stereoselective gem-C,B-Glycosylation via 1,2-Boronate Migration. J Am Chem Soc 2022. [PMID: 35112837 DOI: 10.1021/jacs.1c11842] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Coines J, Cuxart I, Teze D, Rovira C. Computer Simulation to Rationalize “Rational” Engineering of Glycoside Hydrolases and Glycosyltransferases. J Phys Chem B. [DOI: 10.1021/acs.jpcb.1c09536] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
13 Kawanobe Y, Kuragaki N, Tsubomura T, Yamazaki Y, Kuribara T, Totani K. Mechanistic Study of Silyl‐Assist Effect on 1,2‐ cis ‐α‐Glucosylation. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202104152] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Siyabalapitiya Arachchige S, Crich D. Side Chain Conformation and Its Influence on Glycosylation Selectivity in Hexo- and Higher Carbon Furanosides. J Org Chem 2021. [PMID: 34905382 DOI: 10.1021/acs.joc.1c02374] [Reference Citation Analysis]
15 Panova MV, Medvedev MG, Orlova AV, Kononov LO. Exhaustive Conformational Search for Sialyl Cation Reveals Possibility of Remote Participation of Acyl Groups. Chemphyschem 2021;:e202100788. [PMID: 34837303 DOI: 10.1002/cphc.202100788] [Reference Citation Analysis]
16 Upadhyaya K, Subedi YP, Crich D. Direct Experimental Characterization of a Bridged Bicyclic Glycosyl Dioxacarbenium Ion by 1 H and 13 C NMR Spectroscopy: Importance of Conformation on Participation by Distal Esters. Angew Chem Int Ed Engl 2021;60:25397-403. [PMID: 34543505 DOI: 10.1002/anie.202110212] [Reference Citation Analysis]
17 Upadhyaya K, Subedi YP, Crich D. Direct Experimental Characterization of a Bridged Bicyclic Glycosyl Dioxacarbenium Ion by 1 H and 13 C NMR Spectroscopy: Importance of Conformation on Participation by Distal Esters. Angewandte Chemie 2021;133:25601-7. [DOI: 10.1002/ange.202110212] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
18 Loh CCJ. Exploiting non-covalent interactions in selective carbohydrate synthesis. Nat Rev Chem 2021;5:792-815. [DOI: 10.1038/s41570-021-00324-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Lin MH, Chang CW, Chiang TY, Dhurandhare VM, Wang CC. Thiocarbonyl as a Switchable Relay-Auxiliary Group in Carbohydrate Synthesis. Org Lett 2021;23:7313-8. [PMID: 34269593 DOI: 10.1021/acs.orglett.1c01968] [Reference Citation Analysis]
20 Andreana PR, Crich D. Guidelines for O-Glycoside Formation from First Principles. ACS Cent Sci 2021;7:1454-62. [PMID: 34584944 DOI: 10.1021/acscentsci.1c00594] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
21 Puri K, Kulkarni SS. Total Synthesis of the Phosphorylated Zwitterionic Trisaccharide Repeating Unit of Photorhabdus temperata cinerea 3240. Org Lett 2021;23:7083-7. [PMID: 34459612 DOI: 10.1021/acs.orglett.1c02487] [Reference Citation Analysis]
22 Quirke JCK, Crich D. GH47 and Other Glycoside Hydrolases Catalyze Glycosidic Bond Cleavage with the Assistance of Substrate Super-arming at the Transition State. ACS Catal 2021;11:10308-15. [PMID: 34777906 DOI: 10.1021/acscatal.1c02750] [Reference Citation Analysis]
23 Fittolani G, Tyrikos-Ergas T, Vargová D, Chaube MA, Delbianco M. Progress and challenges in the synthesis of sequence controlled polysaccharides. Beilstein J Org Chem 2021;17:1981-2025. [PMID: 34386106 DOI: 10.3762/bjoc.17.129] [Reference Citation Analysis]
24 Upadhyaya K, Bagul RS, Crich D. Influence of Configuration at the 4- and 6-Positions on the Conformation and Anomeric Reactivity and Selectivity of 7-Deoxyheptopyranosyl Donors: Discovery of a Highly Equatorially Selective l-glycero-d-gluco-Heptopyranosyl Donor. J Org Chem 2021;86:12199-225. [PMID: 34343001 DOI: 10.1021/acs.joc.1c01535] [Reference Citation Analysis]
25 Das A, Jayaraman N. Aglycon reactivity as a guiding principle in latent-active approach to chemical glycosylations. Carbohydr Res 2021;508:108404. [PMID: 34352649 DOI: 10.1016/j.carres.2021.108404] [Reference Citation Analysis]
26 Bennett CS. Glycosyl Sulfonates Beyond Triflates. Chem Rec 2021. [PMID: 34142755 DOI: 10.1002/tcr.202100141] [Reference Citation Analysis]
27 Zhu Y, Delbianco M, Seeberger PH. Automated Assembly of Starch and Glycogen Polysaccharides. J Am Chem Soc 2021;143:9758-68. [PMID: 34115468 DOI: 10.1021/jacs.1c02188] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Franconetti A, Ardá A, Asensio JL, Blériot Y, Thibaudeau S, Jiménez-Barbero J. Glycosyl Oxocarbenium Ions: Structure, Conformation, Reactivity, and Interactions. Acc Chem Res 2021;54:2552-64. [PMID: 33930267 DOI: 10.1021/acs.accounts.1c00021] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 13.0] [Reference Citation Analysis]
29 Jayaraman N. Display of Rich Reactivities of Endo- and Exocyclic Unsaturated Sugars that Parallel the Native Sugars. Chem Rec 2021. [PMID: 33960656 DOI: 10.1002/tcr.202100091] [Reference Citation Analysis]
30 Zhang GL, Gadi MR, Cui X, Liu D, Zhang J, Saikam V, Gibbons C, Wang PG, Li L. Protecting-group-free S-glycosylation towards thioglycosides and thioglycopeptides in water. Green Chem 2021;23:2907-12. [PMID: 34497476 DOI: 10.1039/D1GC00098E] [Reference Citation Analysis]
31 Escopy S, Singh Y, Demchenko AV. Palladium(II)-assisted activation of thioglycosides. Org Biomol Chem 2021;19:2044-54. [PMID: 33599667 DOI: 10.1039/d1ob00004g] [Reference Citation Analysis]
32 Smajlagic I, Carlson B, Dudding T. Brønsted Acid Organocatalyzed Three-Component Hydroamidation Reactions of Vinyl Ethers. J Org Chem 2021;86:4171-81. [PMID: 33626274 DOI: 10.1021/acs.joc.0c03017] [Reference Citation Analysis]
33 Muru K, Gauthier C. Glycosylation and Protecting Group Strategies Towards the Synthesis of Saponins and Bacterial Oligosaccharides: A Personal Account. Chem Rec . [DOI: 10.1002/tcr.202000181] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]