Strategies toward protecting group-free glycosylation through selective activation of the anomeric center

被引:40
作者
Downey, A. Michael [1 ]
Hocek, Michal [1 ,2 ]
机构
[1] Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo Nam 2, Prague 16610 6, Czech Republic
[2] Charles Univ Prague, Fac Sci, Dept Organ Chem, Prague 12843 2, Czech Republic
关键词
glycosides; glycosylation; oligosaccharides; protecting groups; ONE-STEP SYNTHESIS; ONE-POT SYNTHESIS; UNPROTECTED 1-THIOIMIDOYL HEXOFURANOSIDES; 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLORIDE; CARBOHYDRATE-CHEMISTRY; ALKYL GLYCOSIDES; REDUCING SUGARS; O-GLYCOSYLATION; P-TOLUENESULFONOHYDRAZIDE; PROTEIN GLYCOCONJUGATION;
D O I
10.3762/bjoc.13.123
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Glycosylation is an immensely important biological process and one that is highly controlled and very efficient in nature. However, in a chemical laboratory the process is much more challenging and usually requires the extensive use of protecting groups to squelch reactivity at undesired reactive moieties. Nonetheless, by taking advantage of the differential reactivity of the anomeric center, a selective activation at this position is possible. As a result, protecting group-free strategies to effect glycosylations are available thanks to the tremendous efforts of many research groups. In this review, we showcase the methods available for the selective activation of the anomeric center on the glycosyl donor and the mechanisms by which the glycosylation reactions take place to illustrate the power these techniques.
引用
收藏
页码:1239 / 1279
页数:41
相关论文
共 118 条
[1]   Non-canonical amino acids as a useful synthetic biological tool for lipase-catalysed reactions in hostile environments [J].
Acevedo-Rocha, Carlos G. ;
Hoesl, Michael G. ;
Nehring, Sebastian ;
Royter, Marina ;
Wolschner, Christina ;
Wiltschi, Birgit ;
Antranikian, Garabed ;
Budisa, Nediljko .
CATALYSIS SCIENCE & TECHNOLOGY, 2013, 3 (05) :1198-1201
[2]   Protecting group free synthesis of glycosyl thiols from reducing sugars in water; application to the production of N-glycan glycoconjugates [J].
Alexander, S. R. ;
Lim, D. ;
Amso, Z. ;
Brimble, M. A. ;
Fairbanks, A. J. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2017, 15 (10) :2152-2156
[3]   Protecting group-free immobilization of glycans for affinity chromatography using glycosylsulfonohydrazide donors [J].
Armada, Daniel Hernandez ;
Santos, Jobette T. ;
Richards, Michele R. ;
Cairo, Christopher W. .
CARBOHYDRATE RESEARCH, 2015, 417 :109-116
[4]   Stereochemistry of nucleophilic substitution reactions depending upon substituent: Evidence for electrostatic stabilization of pseudoaxial conformers of oxocarbenium ions by heteroatom substituents [J].
Ayala, L ;
Lucero, CG ;
Romero, JAC ;
Tabacco, SA ;
Woerpel, KA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (50) :15521-15528
[5]  
Beckmann H. S. G., 2009, Organic Azides, P469, DOI DOI 10.1002/9780470682517.CH16
[6]   The direct formation of glycosyl thiols from reducing sugars allows one-pot protein glycoconjugation [J].
Bernardes, Goncalo J. L. ;
Gamblin, David P. ;
Davis, Benjamin G. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (24) :4007-4011
[7]   A NEW SYNTHESIS OF D-GLYCOSIDURONATES FROM UNPROTECTED D-URONIC ACIDS [J].
BERTHO, JN ;
FERRIERES, V ;
PLUSQUELLEC, D .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (13) :1391-1393
[8]   Structure, activity, synthesis and biosynthesis of aryl-C-glycosides [J].
Bililign, T ;
Griffith, BR ;
Thorson, JS .
NATURAL PRODUCT REPORTS, 2005, 22 (06) :742-760
[9]   A propos of glycosyl cations and the mechanism of chemical glycosylation [J].
Bohe, Luis ;
Crich, David .
COMPTES RENDUS CHIMIE, 2011, 14 (01) :3-16
[10]   Microwave-accelerated Fischer glycosylation [J].
Bornaghi, LF ;
Poulsen, SA .
TETRAHEDRON LETTERS, 2005, 46 (20) :3485-3488