Chemical glycosylation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Chemical glycosylation" in English language version.

refsWebsite

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26doi.org

2^nd place

14nih.gov

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2zenodo.org

621^st place

380^th place

1handle.net

102^nd place

76^th place

1semanticscholar.org

11^th place

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1harvard.edu

18^th place

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1sciencedirect.com

149^th place

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doi.org

Crich, D.; Lim, L. (2004). "Glycosylation with Sulfoxides and Sulfinates as Donors or Promoters". Org. React. 64: 115–251. doi:10.1002/0471264180.or064.02. ISBN 0471264180.
Bufali, S.; Seeberger, P. (2006). "Glycosylation on Polymer Supports". Org. React. 68: 115–251. doi:10.1002/0471264180.or068.02. ISBN 0471264180.
Vorm, Stefan van der; Hansen, Thomas; Hengst, Jacob M. A. van; S. Overkleeft, Herman; Marel, Gijsbert A. van der; C. Codée, Jeroen D. (2019). "Acceptor reactivity in glycosylation reactions". Chemical Society Reviews. 48 (17): 4688–4706. doi:10.1039/C8CS00369F. hdl:1887/79489. PMID 31287452.
Vorm, S. van der; Hansen, T.; S. Overkleeft, H.; Marel, G. A. van der; C. Codée, J. D. (2017). "The influence of acceptor nucleophilicity on the glycosylation reaction mechanism". Chemical Science. 8 (3): 1867–75. doi:10.1039/C6SC04638J. PMC 5424809. PMID 28553477.
Koenigs, Wilhelm; Knorr, Edward (1901). "Ueber einige Derivate des Traubenzuckers und der Galactose (p )". Berichte der deutschen chemischen Gesellschaft. 34 (1): 957–981. doi:10.1002/cber.190103401162.
Fischer, E. (1893). "Ueber die Glucoside der Alkohole". Ber. Dtsch. Chem. Ges. 26 (3): 2400–12. doi:10.1002/cber.18930260327.
Gervay, J.; Hadd, M. J. (1997). "Anionic Additions to Glycosyl Iodides: Highly Stereoselective Syntheses of β C-, N-, and O-Glycosides1". J. Org. Chem. 62 (20): 6961–67. doi:10.1021/jo970922t.
Hadd, M.J.; Gervay, J. (1999). "Glycosyl iodides are highly efficient donors under neutral conditions". Carbohydr. Res. 320 (1–2): 61–69. doi:10.1016/S0008-6215(99)00146-9.
Miquel, N.; Vignando, S.; Russo, G.; Lay, L. (2004). "Efficient Synthesis of O-, S-, N- and C-Glycosides of 2-Amino-2-Deoxy-d-Glucopyranose from Glycosyl Iodides". Synlett. 2004 (2): 341–3. doi:10.1055/s-2003-44978.
van Well, R.M.; Kartha, K.P.R.; Field, R.A. (2005). "Iodine Promoted Glycosylation with Glycosyl Iodides: α-Glycoside Synthesis". J. Carbohydr. Chem. 24 (4–6): 463–474. doi:10.1081/CAR-200067028. S2CID 86329924.
Gervay, J.; Nguyen, T.N.; Hadd, M.J. (1997). "Mechanistic studies on the stereoselective formation of glycosyl iodides: first characterization of β-d-glycosyl iodides". Carbohydr. Res. 300 (2): 119–125. doi:10.1016/S0008-6215(96)00321-7.
Zhu X, Schmidt RR (2009). "New principles for glycoside-bond formation". Angew Chem Int Ed Engl. 48 (11): 1900–34. doi:10.1002/anie.200802036. PMID 19173361.
Lam SN, Gervay-Hague J (October 2003). "Efficient route to 2-deoxy beta-O-aryl-d-glycosides via direct displacement of glycosyl iodides". Org Lett. 5 (22): 4219–22. doi:10.1021/ol035705v. PMID 14572289.
Du W, Gervay-Hague J (May 2005). "Efficient synthesis of alpha-galactosyl ceramide analogues using glycosyl iodide donors". Org Lett. 7 (10): 2063–5. doi:10.1021/ol050659f. PMID 15876055.
Du W, Kulkarni SS, Gervay-Hague J (June 2007). "Efficient, one-pot syntheses of biologically active alpha-linked glycolipids". Chem Commun. 23 (23): 2336–8. doi:10.1039/b702551c. PMID 17844738.
Fischer, E.; Delbrück, K. (1909). "Über Thiophenol-glucoside". Ber. Dtsch. Chem. Ges. 42 (2): 1476–82. doi:10.1002/cber.19090420210.
Tai CA, Kulkarni SS, Hung SC (October 2003). "Facile Cu(OTf)2-catalyzed preparation of per-O-acetylated hexopyranoses with stoichiometric acetic anhydride and sequential one-pot anomeric substitution to thioglycosides under solvent-free conditions". J Org Chem. 68 (22): 8719–22. doi:10.1021/jo030073b. PMID 14575510.
Agnihotri G, Tiwari P, Misra AK (May 2005). "One-pot synthesis of per-O-acetylated thioglycosides from unprotected reducing sugars". Carbohydr Res. 340 (7): 1393–6. doi:10.1016/j.carres.2005.02.027. PMID 15854611.
Hasegawa JY, Hamada M, Miyamoto T, Nishide K, Kajimoto T, Uenishi J, Node M (October 2005). "The application of phenylmethanethiol and benzenethiol derivatives as odorless organosulfur reagents in the synthesis of thiosugars and thioglycosides". Carbohydr Res. 340 (15): 2360–8. doi:10.1016/j.carres.2005.07.011. PMID 16143318.
Veeneman, G.H.; van Leeuwen, S.H.; van Boom, J.H. (1990). "Iodonium ion promoted reactions at the anomeric centre. II an efficient thioglycoside mediated approach toward the formation of 1,2-trans linked glycosides and glycosidic esters". Tetrahedron Lett. 31 (9): 1331–4. doi:10.1016/S0040-4039(00)88799-7.
Schmidt, R.R.; Michel, J. (1980). "Einfache Synthese von α-und β-O-Glykosylimidaten; Herstellung von Glykosiden und Disacchariden". Angew. Chem. 92 (9): 763–4. Bibcode:1980AngCh..92..763S. doi:10.1002/ange.19800920933.
Schmidt, R.R.; Michel, J. (1980). "Facile Synthesis of α- and β-O-Glycosyl Imidates; Preparation of Glycosides and Disaccharides". Angew. Chem. Int. Ed. Engl. 19 (9): 731–2. doi:10.1002/anie.198007311.
Kale RR, McGannon CM, Fuller-Schaefer C, Hatch DM, Flagler MJ, Gamage SD, Weiss AA, Iyer SS (2008). "Differentiation between structurally homologous Shiga 1 and Shiga 2 toxins by using synthetic glycoconjugates". Angew Chem Int Ed Engl. 47 (7): 1265–8. doi:10.1002/anie.200703680. PMID 18172842.
Heuckendorff, Mads; Jensen, Henrik H. (2017). "Removal of some common glycosylation by-products during reaction work-up". Carbohydrate Research. 439: 50–56. doi:10.1016/j.carres.2016.12.007. PMID 28107657.
Joe M, Bai Y, Nacario RC, Lowary TL (August 2007). "Synthesis of the docosanasaccharide arabinan domain of mycobacterial arabinogalactan and a proposed octadecasaccharide biosynthetic precursor". J Am Chem Soc. 129 (32): 9885–901. doi:10.1021/ja072892+. PMID 17655235.
Wu X, Bundle DR (September 2005). "Synthesis of glycoconjugate vaccines for Candida albicans using novel linker methodology". J Org Chem. 70 (18): 7381–8. doi:10.1021/jo051065t. PMID 16122263.

handle.net

hdl.handle.net

Vorm, Stefan van der; Hansen, Thomas; Hengst, Jacob M. A. van; S. Overkleeft, Herman; Marel, Gijsbert A. van der; C. Codée, Jeroen D. (2019). "Acceptor reactivity in glycosylation reactions". Chemical Society Reviews. 48 (17): 4688–4706. doi:10.1039/C8CS00369F. hdl:1887/79489. PMID 31287452.

harvard.edu

ui.adsabs.harvard.edu

Schmidt, R.R.; Michel, J. (1980). "Einfache Synthese von α-und β-O-Glykosylimidaten; Herstellung von Glykosiden und Disacchariden". Angew. Chem. 92 (9): 763–4. Bibcode:1980AngCh..92..763S. doi:10.1002/ange.19800920933.

nih.gov

pubmed.ncbi.nlm.nih.gov

Vorm, Stefan van der; Hansen, Thomas; Hengst, Jacob M. A. van; S. Overkleeft, Herman; Marel, Gijsbert A. van der; C. Codée, Jeroen D. (2019). "Acceptor reactivity in glycosylation reactions". Chemical Society Reviews. 48 (17): 4688–4706. doi:10.1039/C8CS00369F. hdl:1887/79489. PMID 31287452.
Vorm, S. van der; Hansen, T.; S. Overkleeft, H.; Marel, G. A. van der; C. Codée, J. D. (2017). "The influence of acceptor nucleophilicity on the glycosylation reaction mechanism". Chemical Science. 8 (3): 1867–75. doi:10.1039/C6SC04638J. PMC 5424809. PMID 28553477.
Zhu X, Schmidt RR (2009). "New principles for glycoside-bond formation". Angew Chem Int Ed Engl. 48 (11): 1900–34. doi:10.1002/anie.200802036. PMID 19173361.
Lam SN, Gervay-Hague J (October 2003). "Efficient route to 2-deoxy beta-O-aryl-d-glycosides via direct displacement of glycosyl iodides". Org Lett. 5 (22): 4219–22. doi:10.1021/ol035705v. PMID 14572289.
Du W, Gervay-Hague J (May 2005). "Efficient synthesis of alpha-galactosyl ceramide analogues using glycosyl iodide donors". Org Lett. 7 (10): 2063–5. doi:10.1021/ol050659f. PMID 15876055.
Du W, Kulkarni SS, Gervay-Hague J (June 2007). "Efficient, one-pot syntheses of biologically active alpha-linked glycolipids". Chem Commun. 23 (23): 2336–8. doi:10.1039/b702551c. PMID 17844738.
Tai CA, Kulkarni SS, Hung SC (October 2003). "Facile Cu(OTf)2-catalyzed preparation of per-O-acetylated hexopyranoses with stoichiometric acetic anhydride and sequential one-pot anomeric substitution to thioglycosides under solvent-free conditions". J Org Chem. 68 (22): 8719–22. doi:10.1021/jo030073b. PMID 14575510.
Agnihotri G, Tiwari P, Misra AK (May 2005). "One-pot synthesis of per-O-acetylated thioglycosides from unprotected reducing sugars". Carbohydr Res. 340 (7): 1393–6. doi:10.1016/j.carres.2005.02.027. PMID 15854611.
Hasegawa JY, Hamada M, Miyamoto T, Nishide K, Kajimoto T, Uenishi J, Node M (October 2005). "The application of phenylmethanethiol and benzenethiol derivatives as odorless organosulfur reagents in the synthesis of thiosugars and thioglycosides". Carbohydr Res. 340 (15): 2360–8. doi:10.1016/j.carres.2005.07.011. PMID 16143318.
Kale RR, McGannon CM, Fuller-Schaefer C, Hatch DM, Flagler MJ, Gamage SD, Weiss AA, Iyer SS (2008). "Differentiation between structurally homologous Shiga 1 and Shiga 2 toxins by using synthetic glycoconjugates". Angew Chem Int Ed Engl. 47 (7): 1265–8. doi:10.1002/anie.200703680. PMID 18172842.
Heuckendorff, Mads; Jensen, Henrik H. (2017). "Removal of some common glycosylation by-products during reaction work-up". Carbohydrate Research. 439: 50–56. doi:10.1016/j.carres.2016.12.007. PMID 28107657.
Joe M, Bai Y, Nacario RC, Lowary TL (August 2007). "Synthesis of the docosanasaccharide arabinan domain of mycobacterial arabinogalactan and a proposed octadecasaccharide biosynthetic precursor". J Am Chem Soc. 129 (32): 9885–901. doi:10.1021/ja072892+. PMID 17655235.
Wu X, Bundle DR (September 2005). "Synthesis of glycoconjugate vaccines for Candida albicans using novel linker methodology". J Org Chem. 70 (18): 7381–8. doi:10.1021/jo051065t. PMID 16122263.

ncbi.nlm.nih.gov

Vorm, S. van der; Hansen, T.; S. Overkleeft, H.; Marel, G. A. van der; C. Codée, J. D. (2017). "The influence of acceptor nucleophilicity on the glycosylation reaction mechanism". Chemical Science. 8 (3): 1867–75. doi:10.1039/C6SC04638J. PMC 5424809. PMID 28553477.

sciencedirect.com

Heuckendorff, Mads; Jensen, Henrik H. (2017). "Removal of some common glycosylation by-products during reaction work-up". Carbohydrate Research. 439: 50–56. doi:10.1016/j.carres.2016.12.007. PMID 28107657.

semanticscholar.org

api.semanticscholar.org

van Well, R.M.; Kartha, K.P.R.; Field, R.A. (2005). "Iodine Promoted Glycosylation with Glycosyl Iodides: α-Glycoside Synthesis". J. Carbohydr. Chem. 24 (4–6): 463–474. doi:10.1081/CAR-200067028. S2CID 86329924.

zenodo.org

Koenigs, Wilhelm; Knorr, Edward (1901). "Ueber einige Derivate des Traubenzuckers und der Galactose (p )". Berichte der deutschen chemischen Gesellschaft. 34 (1): 957–981. doi:10.1002/cber.190103401162.
Fischer, E. (1893). "Ueber die Glucoside der Alkohole". Ber. Dtsch. Chem. Ges. 26 (3): 2400–12. doi:10.1002/cber.18930260327.