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Items: 1 to 20 of 114

1.

Design of chemical glycosyl donors: does changing ring conformation influence selectivity/reactivity?

Satoh H, Manabe S.

Chem Soc Rev. 2013 May 21;42(10):4297-309. doi: 10.1039/c3cs35457a. Review.

PMID:
23364773
2.

Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation.

Gervay-Hague J.

Acc Chem Res. 2016 Jan 19;49(1):35-47. doi: 10.1021/acs.accounts.5b00357.

PMID:
26524481
3.

Conformationally armed 3,6-tethered glycosyl donors: synthesis, conformation, reactivity, and selectivity.

Heuckendorff M, Pedersen CM, Bols M.

J Org Chem. 2013 Jul 19;78(14):7234-48. doi: 10.1021/jo4012464.

PMID:
23786671
4.

Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions.

Pedersen CM, Marinescu LG, Bols M.

Chem Commun (Camb). 2008 Jun 7;(21):2465-7. doi: 10.1039/b801305e.

PMID:
18491016
5.

Propargyl/methyl furanosides as potential glycosyl donors.

Vidadala SR, Gayatri G, Sastry GN, Hotha S.

Chem Commun (Camb). 2011 Sep 21;47(35):9906-8. doi: 10.1039/c1cc13134f.

PMID:
21818464
6.

Glycosyl trichloroacetylcarbamate: a new glycosyl donor for O-glycosylation.

Jayakanthan K, Vankar YD.

Carbohydr Res. 2005 Dec 12;340(17):2688-92.

PMID:
16212950
7.

Direct experimental evidence for the high chemical reactivity of α- and β-xylopyranosides adopting a (2,5)B conformation in glycosyl transfer.

Amorim L, Marcelo F, Rousseau C, Nieto L, Jiménez-Barbero J, Marrot J, Rauter AP, Sollogoub M, Bols M, Blériot Y.

Chemistry. 2011 Jun 20;17(26):7345-56. doi: 10.1002/chem.201003251.

PMID:
21567492
8.

Endocyclic cleavage in glycosides with 2,3-trans cyclic protecting groups.

Satoh H, Manabe S, Ito Y, Lüthi HP, Laino T, Hutter J.

J Am Chem Soc. 2011 Apr 13;133(14):5610-9. doi: 10.1021/ja201024a.

PMID:
21417469
9.
10.

Superarming of glycosyl donors by combined neighboring and conformational effects.

Heuckendorff M, Premathilake HD, Pornsuriyasak P, Madsen AØ, Pedersen CM, Bols M, Demchenko AV.

Org Lett. 2013 Sep 20;15(18):4904-7. doi: 10.1021/ol402371b.

12.

Assembly of naturally occurring glycosides, evolved tactics, and glycosylation methods.

Yu B, Sun J, Yang X.

Acc Chem Res. 2012 Aug 21;45(8):1227-36. doi: 10.1021/ar200296m. Review.

PMID:
22493991
13.

2,3-Anhydrosugars in glycoside bond synthesis. Application to alpha-D-galactofuranosides.

Bai Y, Lowary TL.

J Org Chem. 2006 Dec 22;71(26):9658-71.

PMID:
17168583
14.
15.

gem-Dimethyl 4-pentenyl glycosides: novel glycosylating agents and anomeric protecting groups.

Fortin M, Kaplan J, Pham K, Kirk S, Andrade RB.

Org Lett. 2009 Aug 20;11(16):3594-7. doi: 10.1021/ol901313z.

PMID:
19634893
16.

Highly stereoselective glycosyl-chloride-mediated synthesis of 2-deoxyglucosides.

Verma VP, Wang CC.

Chemistry. 2013 Jan 14;19(3):846-51. doi: 10.1002/chem.201203418.

PMID:
23233443
18.

O-Benzoxazolyl imidates as versatile glycosyl donors for chemical glycosylation.

Nigudkar SS, Parameswar AR, Pornsuriyasak P, Stine KJ, Demchenko AV.

Org Biomol Chem. 2013 Jun 28;11(24):4068-76. doi: 10.1039/c3ob40667a.

PMID:
23674052
19.

Stereoselective glycosylation using oxathiane glycosyl donors.

Fascione MA, Adshead SJ, Stalford SA, Kilner CA, Leach AG, Turnbull WB.

Chem Commun (Camb). 2009 Oct 21;(39):5841-3. doi: 10.1039/b913308a.

PMID:
19787115
20.

Glycosyl alkoxythioimidates as building blocks for glycosylation: a reactivity study.

Ranade SC, Demchenko AV.

Carbohydr Res. 2015 Feb 11;403:115-22. doi: 10.1016/j.carres.2014.06.025.

PMID:
25043398
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