-
1
-
-
0035937526
-
Glycosylation and the immune system
-
Rudd, P.M.; Elliott, T.; Cresswell, P.; Wilson, I.A.; Dwek, R.A. Glycosylation and the immune system. Science 2001, 291, 2370-2376.
-
(2001)
Science
, vol.291
, pp. 2370-2376
-
-
Rudd, P.M.1
Elliott, T.2
Cresswell, P.3
Wilson, I.A.4
Dwek, R.A.5
-
2
-
-
0035937499
-
Chemical glycobiology
-
Bertozzi, C.R.; Kiessling, L.L. Chemical glycobiology. Science 2001, 291, 2357-2364.
-
(2001)
Science
, vol.291
, pp. 2357-2364
-
-
Bertozzi, C.R.1
Kiessling, L.L.2
-
3
-
-
44849094155
-
The chemical neurobiology of carbohydrates
-
Murrey, H.E.; Hsieh-Wilson, L.C. The chemical neurobiology of carbohydrates. Chem. Rev. 2008,108, 1708-1731.
-
(2008)
Chem. Rev.
, vol.108
, pp. 1708-1731
-
-
Murrey, H.E.1
Hsieh-Wilson, L.C.2
-
4
-
-
48349108296
-
Galactose: A specifically recognized, terminal carbohydrate moiety in biological processes
-
Walker-Nasir, E.; Kaleem, A.; Hoessli, D.C.; Khurshid, A.; Nasir-ud-Din. Galactose: a specifically recognized, terminal carbohydrate moiety in biological processes. Curr. Org. Chem. 2008, 12, 940-956.
-
(2008)
Curr. Org. Chem.
, vol.12
, pp. 940-956
-
-
Walker-Nasir, E.1
Kaleem, A.2
Hoessli, D.C.3
Khurshid, A.4
Nasir-Ud-Din5
-
5
-
-
33750974435
-
Cell type-specific roles of carbohydrates in tumor metastasis
-
Chen, S.; Fukuda, M. Cell type-specific roles of carbohydrates in tumor metastasis. Methods Enzymol. 2006, 416, 371-380.
-
(2006)
Methods Enzymol.
, vol.416
, pp. 371-380
-
-
Chen, S.1
Fukuda, M.2
-
6
-
-
0040657616
-
Advances in selective chemical syntheses of complex oligosaccharides
-
Paulsen, H. Advances in selective chemical syntheses of complex oligosaccharides. Angew. Chem. Int. Ed. 1982, 21, 155-173.
-
(1982)
Angew. Chem. Int. Ed.
, vol.21
, pp. 155-173
-
-
Paulsen, H.1
-
7
-
-
0035937463
-
Toward automated synthesis of oligosaccharides and glycoproteins
-
Sears, P.; Wong, C.H. Toward automated synthesis of oligosaccharides and glycoproteins. Science 2001, 291, 2344-2350.
-
(2001)
Science
, vol.291
, pp. 2344-2350
-
-
Sears, P.1
Wong, C.H.2
-
8
-
-
34547337747
-
Oligosaccharide assembly by one-pot multi-step strategy
-
Wang, Y.H.; Ye, X.S.; Zhang, L.H. Oligosaccharide assembly by one-pot multi-step strategy. Org. Biomol. Chem. 2007, 5, 2189-2200.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 2189-2200
-
-
Wang, Y.H.1
Ye, X.S.2
Zhang, L.H.3
-
9
-
-
65449145156
-
Solid-phase synthesis of oligosaccharide drugs: A review
-
Dhanawat, M.; Shrivastava, S.K. Solid-phase synthesis of oligosaccharide drugs: a review. Mini-Rev. Med. Chem. 2009, 9, 169-185.
-
(2009)
Mini-Rev. Med. Chem.
, vol.9
, pp. 169-185
-
-
Dhanawat, M.1
Shrivastava, S.K.2
-
10
-
-
66249093859
-
Oligosaccharide synthesis: From conventional methods to modern expeditious strategies
-
Smoot, J.T.; Demchenko, A.V. Oligosaccharide synthesis: from conventional methods to modern expeditious strategies. Adv. Carbohydr. Chem. Biochem. 2009, 62, 161-250.
-
(2009)
Adv. Carbohydr. Chem. Biochem.
, vol.62
, pp. 161-250
-
-
Smoot, J.T.1
Demchenko, A.V.2
-
11
-
-
34347270512
-
Automated solid phase oligosaccharide synthesis
-
Braese, S., Ed.; Springer-Verlag: Berlin, Germany
-
Castagner, B.; Seeberger, P.H. Automated solid phase oligosaccharide synthesis. In Combinatorial Chemistry on Solid Supports; Braese, S., Ed.; Springer-Verlag: Berlin, Germany, 2007; Volume 278, pp. 289-309.
-
(2007)
Combinatorial Chemistry on Solid Supports
, vol.278
, pp. 289-309
-
-
Castagner, B.1
Seeberger, P.H.2
-
12
-
-
6344258876
-
Synthesis of heparin-like oligosaccharides on polymer supports
-
Ojeda, R.; Terenti, O.; de Paz, J.L.; Martin-Lomas, M. Synthesis of heparin-like oligosaccharides on polymer supports. Glycoconjugate J. 2004, 21, 179-195.
-
(2004)
Glycoconjugate J.
, vol.21
, pp. 179-195
-
-
Ojeda, R.1
Terenti, O.2
De Paz, J.L.3
Martin-Lomas, M.4
-
13
-
-
70350441377
-
Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research
-
Boltje, T.J.; Buskas, T.; Boons, G.J. Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research. Nat. Chem. 2009, 1, 611-622.
-
(2009)
Nat. Chem.
, vol.1
, pp. 611-622
-
-
Boltje, T.J.1
Buskas, T.2
Boons, G.J.3
-
14
-
-
61849111654
-
New principles for glycoside-bond formation
-
Zhu, X.M.; Schmidt, R.R. New principles for glycoside-bond formation. Angew. Chem. Int. Ed. 2009, 48, 1900-1934.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 1900-1934
-
-
Zhu, X.M.1
Schmidt, R.R.2
-
15
-
-
33646875480
-
Strategies of synthetic methodologies for constructing β-mannosidic linkage
-
El Ashry, E.S.H.; Rashed, N.; Ibrahim, E.S.I. Strategies of synthetic methodologies for constructing β-mannosidic linkage. Curr. Org. Synth. 2005, 2, 175-213.
-
(2005)
Curr. Org. Synth.
, vol.2
, pp. 175-213
-
-
El Ashry, E.S.H.1
Rashed, N.2
Ibrahim, E.S.I.3
-
16
-
-
33846519966
-
Recent trends in the synthesis of O-glycosides of 2-amino-2-deoxysugars
-
Bongat, A.; Demchenko, A.V. Recent trends in the synthesis of O-glycosides of 2-amino-2-deoxysugars. Carbohydr. Res. 2007, 342, 374-406.
-
(2007)
Carbohydr. Res.
, vol.342
, pp. 374-406
-
-
Bongat, A.1
Demchenko, A.V.2
-
17
-
-
46549089246
-
C-5 modifications in N-acetyl-neuraminic acid: Scope and limitations
-
De Meo, C.; Priyadarshani, U. C-5 modifications in N-acetyl-neuraminic acid: scope and limitations. Carbohydr. Res. 2008, 343, 1540-1552.
-
(2008)
Carbohydr. Res.
, vol.343
, pp. 1540-1552
-
-
De Meo, C.1
Priyadarshani, U.2
-
18
-
-
9144248740
-
Sialic acid donors: Chemical synthesis and glycosylation
-
Ress, D.K.; Linhardt, R.J. Sialic acid donors: Chemical synthesis and glycosylation. Curr. Org. Synth. 2004, 1, 31-46.
-
(2004)
Curr. Org. Synth.
, vol.1
, pp. 31-46
-
-
Ress, D.K.1
Linhardt, R.J.2
-
19
-
-
73249133727
-
Recent advances in sialylation
-
Liang, F.F.; Chen, L.; Xing, G.W. Recent advances in sialylation. Chin. J. Org. Chem. 2009, 29, 1317-1324.
-
(2009)
Chin. J. Org. Chem.
, vol.29
, pp. 1317-1324
-
-
Liang, F.F.1
Chen, L.2
Xing, G.W.3
-
20
-
-
0034511734
-
Recent advances in O-sialylation
-
Boons, G.J.; Demchenko, A.V. Recent advances in O-sialylation. Chem. Rev. 2000, 100, 4539-4566.
-
(2000)
Chem. Rev.
, vol.100
, pp. 4539-4566
-
-
Boons, G.J.1
Demchenko, A.V.2
-
21
-
-
0037423110
-
Remote control of α- or β-stereoselectivity in (1→3)-glucosylations in the presence of a C-2 ester capable of neighboring-group participation
-
Zeng, Y.; Ning, J.; Kong, F. Remote control of α- or β-stereoselectivity in (1→3)-glucosylations in the presence of a C-2 ester capable of neighboring-group participation. Carbohydr. Res. 2003, 338, 307-311.
-
(2003)
Carbohydr. Res.
, vol.338
, pp. 307-311
-
-
Zeng, Y.1
Ning, J.2
Kong, F.3
-
22
-
-
0037071176
-
Pure α-linked products can be obtained in high yields in glycosylation with glucosyl trichloroacetimidate donors with a C2 ester capable of neighboring group participation
-
Zeng, Y.; Ning, J.; Kong, F. Pure α-linked products can be obtained in high yields in glycosylation with glucosyl trichloroacetimidate donors with a C2 ester capable of neighboring group participation. Tetrahedron Lett. 2002, 43, 3729-3733.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3729-3733
-
-
Zeng, Y.1
Ning, J.2
Kong, F.3
-
23
-
-
0030662091
-
Coupling of glycal derived thioethyl glycosyl donors with glycal acceptors. An advance in the scope of the glycal assembly
-
Seeberger, P.H.; Eckhardt, M.; Gutteridge, C.E.; Danishefsky, S.J. Coupling of glycal derived thioethyl glycosyl donors with glycal acceptors. An advance in the scope of the glycal assembly. J. Am. Chem. Soc. 1997, 119, 10064-10072.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 10064-10072
-
-
Seeberger, P.H.1
Eckhardt, M.2
Gutteridge, C.E.3
Danishefsky, S.J.4
-
24
-
-
17144386913
-
4-Acetoxy-2,2-dimethylbutanoate: A useful carbohydrate protecting group for the selective formation of β-(1→3)-D-glucans
-
Yu, H.; Williams, D.L.; Ensley, H.E. 4-Acetoxy-2,2-dimethylbutanoate: a useful carbohydrate protecting group for the selective formation of β-(1→3)-D-glucans. Tetrahedron Lett. 2005, 46, 3417-3421.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3417-3421
-
-
Yu, H.1
Williams, D.L.2
Ensley, H.E.3
-
25
-
-
34247472630
-
Stereocontrolled glycoside and glycosyl ester synthesis. Neighboring group participation and hydrogenolysis of 3-(2'-Benzyloxyphenyl)-3,3- dimethylpropanoates
-
Crich, D.; Cai, F. Stereocontrolled glycoside and glycosyl ester synthesis. Neighboring group participation and hydrogenolysis of 3-(2'-Benzyloxyphenyl)-3,3-dimethylpropanoates. Org. Lett. 2007, 9, 1613-1615.
-
(2007)
Org. Lett.
, vol.9
, pp. 1613-1615
-
-
Crich, D.1
Cai, F.2
-
26
-
-
62749144471
-
Methylsulfonylethoxycarbonyl (Msc) and fluorous propylsulfonylethoxycarbonyl (Fpsc) as hydroxy-protecting groups in carbohydrate chemistry
-
Ali, A.; van den Berg, R.; Overkleeft, H.S.; Filippov, D.V.; van der Marel, G.A.; Codee, J. Methylsulfonylethoxycarbonyl (Msc) and fluorous propylsulfonylethoxycarbonyl (Fpsc) as hydroxy-protecting groups in carbohydrate chemistry. Tetrahedron Lett. 2009, 50, 2185-2188.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2185-2188
-
-
Ali, A.1
Van Den Berg, R.2
Overkleeft, H.S.3
Filippov, D.V.4
Van Der Marel, G.A.5
Codee, J.6
-
27
-
-
33845219373
-
Dialkylphosphates as stereodirecting protecting groups in oligosaccharide synthesis
-
Yamada, T.; Takemura, K.; Yoshida, J.; Yamago, S. Dialkylphosphates as stereodirecting protecting groups in oligosaccharide synthesis. Angew. Chem. Int. Ed. 2006, 45, 7575-7578.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7575-7578
-
-
Yamada, T.1
Takemura, K.2
Yoshida, J.3
Yamago, S.4
-
28
-
-
0030684114
-
19F NMR spectroscopic investigation
-
19F NMR spectroscopic investigation. J. Am. Chem. Soc. 1997, 119, 11217-11223.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 11217-11223
-
-
Crich, D.1
Sun, S.2
-
29
-
-
33845280670
-
Armed and disarmed n-pentenyl glycosides in saccharide couplings leading to oligosaccharides
-
Mootoo, D.R.; Konradsson, P.; Udodong, U.; Fraser-Reid, B. Armed and disarmed n-pentenyl glycosides in saccharide couplings leading to oligosaccharides. J. Am. Chem. Soc. 1988, 110, 5583-5584.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 5583-5584
-
-
Mootoo, D.R.1
Konradsson, P.2
Udodong, U.3
Fraser-Reid, B.4
-
30
-
-
85022498621
-
N-Pentenyl glycosides in organic chemistry: A contemporary example of serendipity
-
Fraser-Reid, B.; Udodong, U.E.; Wu, Z.; Ottosson, H.; Merritt, J.R.; Rao, C.S.; Roberts, C.; Madsen, R. n-Pentenyl glycosides in organic chemistry: a contemporary example of serendipity. Synlett 1992, 927-942.
-
(1992)
Synlett
, pp. 927-942
-
-
Fraser-Reid, B.1
Udodong, U.E.2
Wu, Z.3
Ottosson, H.4
Merritt, J.R.5
Rao, C.S.6
Roberts, C.7
Madsen, R.8
-
31
-
-
27744505650
-
Development of an arming participating group for stereoselective glycosylation and chemoselective oligosaccharide synthesis
-
Smoot, J.T.; Pornsuriyasak, P.; Demchenko, A.V. Development of an arming participating group for stereoselective glycosylation and chemoselective oligosaccharide synthesis. Angew. Chem. Int. Ed. 2005, 44, 7123-7126.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 7123-7126
-
-
Smoot, J.T.1
Pornsuriyasak, P.2
Demchenko, A.V.3
-
32
-
-
13744262178
-
Stereoselective glycosylation reactions with chiral auxiliaries
-
Kim, J.H.; Yang, H.; Boons, G.J. Stereoselective glycosylation reactions with chiral auxiliaries. Angew. Chem. Int. Ed. 2005, 44, 947-949.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 947-949
-
-
Kim, J.H.1
Yang, H.2
Boons, G.J.3
-
33
-
-
36849052367
-
Stereoselective glycosylations using chiral auxiliaries
-
Demchenko, A.V., Ed.; American Chemical Society: Washington, DC, USA
-
Kim, J.H.; Yang, H.; Boons, G.J. Stereoselective glycosylations using chiral auxiliaries. In Frontiers in Modern Carbohydrate Chemistry; Demchenko, A.V., Ed.; American Chemical Society: Washington, DC, USA, 2007; Volume 960, pp. 73-90.
-
(2007)
Frontiers in Modern Carbohydrate Chemistry
, vol.960
, pp. 73-90
-
-
Kim, J.H.1
Yang, H.2
Boons, G.J.3
-
34
-
-
24144498474
-
A general strategy for stereoselective glycosylations
-
Kim, J.; Yang, H.; Park, J.; Boons, G. A general strategy for stereoselective glycosylations. J. Am. Chem. Soc. 2005, 127, 12090-12097.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 12090-12097
-
-
Kim, J.1
Yang, H.2
Park, J.3
Boons, G.4
-
35
-
-
0022260876
-
Human natural anti-α-galactosyl IgG. II. The specific recognition of α-(1→3)-linked galactose residues
-
Galili, U.; Macher, B.A.; Buehler, J.; Shohet, S.B. Human natural anti-α-galactosyl IgG. II. The specific recognition of α-(1→3)-linked galactose residues. J. Exp. Med. 1985, 162, 573-582.
-
(1985)
J. Exp. Med.
, vol.162
, pp. 573-582
-
-
Galili, U.1
Macher, B.A.2
Buehler, J.3
Shohet, S.B.4
-
36
-
-
77954007720
-
Chiral-auxiliary-mediated 1,2-cis-glycosylations for the solid-supported synthesis of a biologically important branched α-glucan
-
Boltje, T.J.; Kim, J.; Park, J.; Boons, G.J. Chiral-auxiliary-mediated 1,2-cis-glycosylations for the solid-supported synthesis of a biologically important branched α-glucan. Nat. Chem. 2010, 2, 552-557.
-
(2010)
Nat. Chem.
, vol.2
, pp. 552-557
-
-
Boltje, T.J.1
Kim, J.2
Park, J.3
Boons, G.J.4
-
37
-
-
32044435384
-
Isolation and structural characterization of an immune-stimulating polysaccharide from fuzi, Aconitum carmichaeli
-
Zhao, C.; Li, M.; Luo, Y.; Wu, W. Isolation and structural characterization of an immune-stimulating polysaccharide from fuzi, Aconitum carmichaeli. Carbohydr. Res. 2006, 341, 485-491.
-
(2006)
Carbohydr. Res.
, vol.341
, pp. 485-491
-
-
Zhao, C.1
Li, M.2
Luo, Y.3
Wu, W.4
-
38
-
-
34447103171
-
Synthesis of N-linked glycan derived from Gram-negative bacterium, Campylobacter jejuni
-
Amin, M.N.; Ishiwata, A.; Ito, Y. Synthesis of N-linked glycan derived from Gram-negative bacterium, Campylobacter jejuni. Tetrahedron 2007, 63, 8181-8198.
-
(2007)
Tetrahedron
, vol.63
, pp. 8181-8198
-
-
Amin, M.N.1
Ishiwata, A.2
Ito, Y.3
-
39
-
-
12944303102
-
Stereoselective glycosylation using the long-range effect of a [2-(4-phenylbenzyl)oxycarbonyl]benzoyl group
-
Tokimoto, H.; Fujimoto, Y.; Fukase, K.; Kusumotot, S. Stereoselective glycosylation using the long-range effect of a [2-(4-phenylbenzyl)oxycarbonyl] benzoyl group. Tetrahedron: Asymmetry 2005, 16, 441-447.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 441-447
-
-
Tokimoto, H.1
Fujimoto, Y.2
Fukase, K.3
Kusumotot, S.4
-
41
-
-
0033520244
-
Stereoselective 1,2-cis-galactosylation assisted by remote neighboring group participation and solvent effects
-
Demchenko, A.V.; Rousson, E.; Boons, G.J. Stereoselective 1,2-cis-galactosylation assisted by remote neighboring group participation and solvent effects. Tetrahedron Lett. 1999, 40, 6523-6526.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 6523-6526
-
-
Demchenko, A.V.1
Rousson, E.2
Boons, G.J.3
-
42
-
-
0001740414
-
Highly stereoselective synthesis of 2'-deoxy-α-ribonucleosides and 2-deoxy-α-C-ribofuranosides by remote stereocontrolled glycosylation
-
Mukaiyama, T.; Ishikawa, T.; Uchiro, H. Highly stereoselective synthesis of 2'-deoxy-α- ribonucleosides and 2-deoxy-α-C-ribofuranosides by remote stereocontrolled glycosylation. Chem. Lett. 1997, 26, 389-390.
-
(1997)
Chem. Lett.
, vol.26
, pp. 389-390
-
-
Mukaiyama, T.1
Ishikawa, T.2
Uchiro, H.3
-
43
-
-
0033520244
-
Stereoselective 1,2-cis-galactosylation assisted by remote neighboring group participation and solvent effects
-
Demchenko, A.V.; Rousson, E.; Boons, G.-J. Stereoselective 1,2-cis-galactosylation assisted by remote neighboring group participation and solvent effects. Tetrahedron Lett. 1999, 40, 6523-6526.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 6523-6526
-
-
Demchenko, A.V.1
Rousson, E.2
Boons, G.-J.3
-
44
-
-
0037403624
-
Pentafluoropropionyl and trifluoroacetyl groups for temporary hydroxyl group protection in oligomannoside synthesis
-
Takatani, M.; Matsuo, I.; Ito, Y. Pentafluoropropionyl and trifluoroacetyl groups for temporary hydroxyl group protection in oligomannoside synthesis. Carbohydr. Res. 2003. 338, 1073-1081.
-
(2003)
Carbohydr. Res.
, vol.338
, pp. 1073-1081
-
-
Takatani, M.1
Matsuo, I.2
Ito, Y.3
-
45
-
-
55449123954
-
Direct and stereoselective synthesis of α-linked 2-deoxyglycosides
-
Park, J.; Boltje, T.J.; Boons, G.J. Direct and stereoselective synthesis of α-linked 2-deoxyglycosides. Org. Lett. 2008, 10, 4367-4370.
-
(2008)
Org. Lett.
, vol.10
, pp. 4367-4370
-
-
Park, J.1
Boltje, T.J.2
Boons, G.J.3
-
46
-
-
3042758507
-
Benzylidene acetal fragmentation route to 6-deoxy sugars: Direct reductive cleavage in the presence of ether protecting groups, permitting the efficient, highly stereocontrolled synthesis of β-D-rhamnosides from D-mannosyl glycosyl donors
-
Crich, D.; Yao, Q.L. Benzylidene acetal fragmentation route to 6-deoxy sugars: Direct reductive cleavage in the presence of ether protecting groups, permitting the efficient, highly stereocontrolled synthesis of β-D-rhamnosides from D-mannosyl glycosyl donors. Total synthesis of a-D-Gal-(1→3)-a-D-Rha-(1→3)-β-D-Rha-(1→4)-β-D-Glu-OMe, the repeating unit of the antigenic lipopolysaccharide from Escherichia hermannii ATCC 33650 and 33652. J. Am. Chem. Soc. 2004, 126, 8232-8236.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8232-8236
-
-
Crich, D.1
Yao, Q.L.2
-
47
-
-
0037067323
-
1 core trisaccharide as a probe for the generality of 1-(benzenesulfinyl)piperidine/triflic anhydride combination for glycosidic bond formation from thioglycosides
-
1 core trisaccharide as a probe for the generality of 1-(benzenesulfinyl)piperidine/ triflic anhydride combination for glycosidic bond formation from thioglycosides. J. Org. Chem. 2002, 67, 4640-4646.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 4640-4646
-
-
Crich, D.1
Li, H.2
-
48
-
-
0030894278
-
Direct synthesis of β-mannopyranosides by the sulfoxide method
-
Crich, D.; Sun, S. Direct synthesis of β-mannopyranosides by the sulfoxide method. J. Org. Chem.1997, 62, 1198-1199.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1198-1199
-
-
Crich, D.1
Sun, S.2
-
49
-
-
0000734076
-
Formation of β-mannopyranosides of primary alcohols using the sulfoxide method
-
Crich, D.; Sun, S. Formation of β-mannopyranosides of primary alcohols using the sulfoxide method. J. Org. Chem. 1996, 61, 4506-4507.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4506-4507
-
-
Crich, D.1
Sun, S.2
-
50
-
-
0034629293
-
Highly diastereoselective α-mannopyranosylation in the absence of participating protecting groups
-
Crich, D.; Cai, W.L.; Dai, Z.M. Highly diastereoselective α-mannopyranosylation in the absence of participating protecting groups. J. Org. Chem. 2000, 65, 1291-1297.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 1291-1297
-
-
Crich, D.1
Cai, W.L.2
Dai, Z.M.3
-
51
-
-
34447294224
-
Direct stereocontrolled synthesis of 3-amino-3-deoxy-β- mannopyranosides: Importance of the nitrogen protecting group on stereoselectivity
-
Crich, D.; Xu, H.D. Direct stereocontrolled synthesis of 3-amino-3-deoxy-β-mannopyranosides: Importance of the nitrogen protecting group on stereoselectivity. J. Org. Chem. 2007, 72, 5183-5192.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 5183-5192
-
-
Crich, D.1
Xu, H.D.2
-
52
-
-
56449107513
-
Does neighboring group participation by non-vicinal esters play a role in glycosylation reactions? Effective probes for the detection of bridging intermediates
-
Crich, D.; Hu, T.S.; Cai, F. Does neighboring group participation by non-vicinal esters play a role in glycosylation reactions? Effective probes for the detection of bridging intermediates. J. Org. Chem. 2008, 73, 8942-8953.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 8942-8953
-
-
Crich, D.1
Hu, T.S.2
Cai, F.3
-
53
-
-
72249090212
-
β-Directing effect of electron-withdrawing groups at O-3,O-4, and O-6 positions and α-directing effect by remote participation of 3-O-acyl and 6-Oacetyl groups of donors in Mannopyranosylations
-
Baek, J.Y.; Lee, B.; Jo, M.G.; Kim, K.S. β-Directing effect of electron-withdrawing groups at O-3,O-4, and O-6 positions and α-directing effect by remote participation of 3-O-acyl and 6-Oacetyl groups of donors in Mannopyranosylations. J. Am. Chem. Soc. 2009, 131, 17705-17713.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 17705-17713
-
-
Baek, J.Y.1
Lee, B.2
Jo, M.G.3
Kim, K.S.4
-
54
-
-
33846553628
-
The use of cyclic bifunctional protecting groups in oligosaccharide synthesis - An overview
-
Litjens, R.; van den Bos, L.J.; Codee, J.; Overkleeft, H.S.; van der Marel, G.A. The use of cyclic bifunctional protecting groups in oligosaccharide synthesis - an overview. Carbohydr. Res. 2007, 342, 419-429.
-
(2007)
Carbohydr. Res.
, vol.342
, pp. 419-429
-
-
Litjens, R.1
Van Den Bos, L.J.2
Codee, J.3
Overkleeft, H.S.4
Van Der Marel, G.A.5
-
55
-
-
7244245511
-
Mechanism of 4,6-O-benzylidene-directed β-mannosylation as determined by α-deuterium kinetic isotope effects
-
Crich, D.; Chandrasekera, N.S. Mechanism of 4,6-O-benzylidene-directed β-mannosylation as determined by α-deuterium kinetic isotope effects. Angew. Chem. Int. Ed. 2004, 43, 5386-5389.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5386-5389
-
-
Crich, D.1
Chandrasekera, N.S.2
-
56
-
-
3342978155
-
The disarming effect of the 4,6-acetal group on glycoside reactivity: Torsional or electronic
-
Jensen, H.H.; Nordstrøm, L.U.; Bols, M. The disarming effect of the 4,6-acetal group on glycoside reactivity: torsional or electronic? J. Am. Chem. Soc. 2004, 126, 9205-9213.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 9205-9213
-
-
Jensen, H.H.1
Nordstrøm, L.U.2
Bols, M.3
-
57
-
-
6044261547
-
Iterative one-pot synthesis of oligosaccharides
-
Huang, X.; Huang, L.; Wang, H.; Ye, X.S. Iterative one-pot synthesis of oligosaccharides. Angew. Chem. Int. Ed. 2004, 43, 5221-5224.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 5221-5224
-
-
Huang, X.1
Huang, L.2
Wang, H.3
Ye, X.S.4
-
58
-
-
77955700674
-
Mechanism of a chemical glycosylation reaction
-
Crich, D. Mechanism of a chemical glycosylation reaction. Acc. Chem. Res. 2010, 43, 1144-1153.
-
(2010)
Acc. Chem. Res.
, vol.43
, pp. 1144-1153
-
-
Crich, D.1
-
59
-
-
33750282565
-
1-Naphthylpropargyl ether group: A readily cleaved and sterically minimal protecting system for stereoselective glycosylation
-
Crich, D.; Wu, B. 1-Naphthylpropargyl ether group: A readily cleaved and sterically minimal protecting system for stereoselective glycosylation. Org. Lett. 2006, 8, 4879-4882.
-
(2006)
Org. Lett.
, vol.8
, pp. 4879-4882
-
-
Crich, D.1
Wu, B.2
-
60
-
-
33645773856
-
Enhanced diastereoselectivity in β-mannopyranosylation through the use of sterically minimal propargyl ether protecting groups
-
Crich, D.; Jayalath, P.; Hutton, T.K. Enhanced diastereoselectivity in β-mannopyranosylation through the use of sterically minimal propargyl ether protecting groups. J. Org. Chem. 2006, 71, 3064-3070.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 3064-3070
-
-
Crich, D.1
Jayalath, P.2
Hutton, T.K.3
-
61
-
-
23044453589
-
Efficient installation of β-mannosides using a dehydrative coupling strategy
-
Codée, J.D.C.; Hossain, L.H.; Seeberger, P.H. Efficient installation of β-mannosides using a dehydrative coupling strategy. Org. Lett. 2005, 7, 3251-3254.
-
(2005)
Org. Lett.
, vol.7
, pp. 3251-3254
-
-
Codée, J.D.C.1
Hossain, L.H.2
Seeberger, P.H.3
-
62
-
-
34250812517
-
Mechanistic studies on the stereoselective formation of β-mannosides from mannosyl iodides using α-deuterium kinetic isotope effects
-
El-Badri, M.H.; Willenbring, D.; Tantillo, D.J.; Gervay-Hague, J. Mechanistic studies on the stereoselective formation of β-mannosides from mannosyl iodides using α-deuterium kinetic isotope effects. J. Org. Chem. 2007, 72, 4663-4672.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 4663-4672
-
-
El-Badri, M.H.1
Willenbring, D.2
Tantillo, D.J.3
Gervay-Hague, J.4
-
63
-
-
26244435768
-
Direct and stereoselective synthesis of β-D-mannosides using 4,6-O-benzylidene-protected mannosyl diethyl phosphite as a donor
-
Tsuda, T.; Arihara, R.; Sato, S.; Koshiba, M.; Nakamura, S.; Hashimoto, S. Direct and stereoselective synthesis of β-D-mannosides using 4,6-O-benzylidene-protected mannosyl diethyl phosphite as a donor. Tetrahedron 2005, 61, 10719-10733.
-
(2005)
Tetrahedron
, vol.61
, pp. 10719-10733
-
-
Tsuda, T.1
Arihara, R.2
Sato, S.3
Koshiba, M.4
Nakamura, S.5
Hashimoto, S.6
-
64
-
-
33751192822
-
A highly reactive and stereoselective β-mannopyranosylation system: Mannosyl 4-pentenoate/PhSeOTf
-
Baek, J.Y.; Choi, T.J.; Jeon, H.B.; Kim, K.S. A highly reactive and stereoselective β-mannopyranosylation system: mannosyl 4-pentenoate/ PhSeOTf. Angew. Chem. Int. Ed. 2006, 45, 7436-7440.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 7436-7440
-
-
Baek, J.Y.1
Choi, T.J.2
Jeon, H.B.3
Kim, K.S.4
-
65
-
-
0034702545
-
An unusual example of steric buttressing in glycosylation
-
Crich, D.; Dudkin, V. An unusual example of steric buttressing in glycosylation. Tetrahedron Lett. 2000, 41, 5643-5646.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 5643-5646
-
-
Crich, D.1
Dudkin, V.2
-
66
-
-
20444480974
-
2-O-Propargyl Ethers: Readily cleavable, minimally intrusive protecting groups for β-mannosyl donors
-
Crich, D.; Jayalath, P. 2-O-Propargyl Ethers: Readily cleavable, minimally intrusive protecting groups for β-mannosyl donors. Org. Lett. 2005, 7, 2277-2280.
-
(2005)
Org. Lett.
, vol.7
, pp. 2277-2280
-
-
Crich, D.1
Jayalath, P.2
-
67
-
-
46849083961
-
Application of the 4-trifluoromethylbenzenepropargyl ether group as an unhindered, electron deficient protecting group for stereoselective glycosylation
-
Crich, D.; Karatholuvhu, M.S. Application of the 4- trifluoromethylbenzenepropargyl ether group as an unhindered, electron deficient protecting group for stereoselective glycosylation. J. Org. Chem. 2008, 73, 5173-5176.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 5173-5176
-
-
Crich, D.1
Karatholuvhu, M.S.2
-
68
-
-
33749013248
-
Synthesis of a β-(1→3)-D-rhamnotetraose by a one-pot, multiple radical fragmentation
-
Crich, D.; Bowers, A.A. Synthesis of a β-(1→3)-D-rhamnotetraose by a one-pot, multiple radical fragmentation. Org. Lett. 2006, 8, 4327-4330.
-
(2006)
Org. Lett.
, vol.8
, pp. 4327-4330
-
-
Crich, D.1
Bowers, A.A.2
-
69
-
-
0141854070
-
The 4,6-O-[α-(2-(2-iodophenyl)ethylthiocarbonyl)benzylidene] protecting group: Stereoselective glycosylation, reductive radical fragmentation, and synthesis of β-D-rhamnopyranosides and other deoxy sugars
-
Crich, D.; Yao, Q.J. The 4,6-O-[α-(2-(2-iodophenyl) ethylthiocarbonyl)benzylidene] protecting group: stereoselective glycosylation, reductive radical fragmentation, and synthesis of β-D-rhamnopyranosides and other deoxy sugars. Org. Lett. 2003, 5, 2189-2191.
-
(2003)
Org. Lett.
, vol.5
, pp. 2189-2191
-
-
Crich, D.1
Yao, Q.J.2
-
70
-
-
0033603525
-
Chemistry of 4,6-O-benzylidene-D-glycopyranosyl triflates: Contrasting behavior between the gluco and manno series
-
Crich, D.; Cai, W. Chemistry of 4,6-O-benzylidene-D-glycopyranosyl triflates: contrasting behavior between the gluco and manno series. J. Org. Chem. 1999, 64, 4926-4930.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 4926-4930
-
-
Crich, D.1
Cai, W.2
-
71
-
-
33750439151
-
On the Influence of the C2-O2 and C3-O3 bonds in 4,6-O-benzylidene- directed β-mannopyranosylation and α-glucopyranosylation
-
Crich, D.; Vinogradova, O. On the Influence of the C2-O2 and C3-O3 bonds in 4,6-O-benzylidene-directed β-mannopyranosylation and α-glucopyranosylation. J. Org. Chem. 2006, 71, 8473-8480.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8473-8480
-
-
Crich, D.1
Vinogradova, O.2
-
72
-
-
0037471444
-
Unusual α-glycosylation with galactosyl donors with a C2 ester capable of neighboring group participation
-
Chen, L.; Kong, F. Unusual α-glycosylation with galactosyl donors with a C2 ester capable of neighboring group participation. Tetrahedron Lett. 2003, 44, 3691-3695.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3691-3695
-
-
Chen, L.1
Kong, F.2
-
73
-
-
24144468638
-
Stereocontrolled formation of β-glucosides and related linkages in the absence of neighboring group participation: Influence of a trans-fused 2,3-O-carbonate group
-
Crich, D.; Jayalath, P. Stereocontrolled formation of β-glucosides and related linkages in the absence of neighboring group participation: Influence of a trans-fused 2,3-O-carbonate group. J. Org. Chem. 2005, 70, 7252-7259.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 7252-7259
-
-
Crich, D.1
Jayalath, P.2
-
74
-
-
53849109813
-
Highly direct α-selective glycosylations of 3,4-O-carbonate- protected 2-deoxy- and 2,6-dideoxythioglycosides by preactivation protocol
-
Lu, Y.S.; Li, Q.; Wang, Y.H.; Ye, X.S. Highly direct α-selective glycosylations of 3,4-O-carbonate-protected 2-deoxy- and 2,6- dideoxythioglycosides by preactivation protocol. Org. Lett. 2008, 10, 3445-3448.
-
(2008)
Org. Lett.
, vol.10
, pp. 3445-3448
-
-
Lu, Y.S.1
Li, Q.2
Wang, Y.H.3
Ye, X.S.4
-
75
-
-
77953238348
-
Direct α-selective glycosylations of acetyl-protected 2-deoxy- and 2,6-dideoxythioglycosides by preactivation protocol
-
Lu, Y.S.; Li, Q.; Wang, Y.H.; Ye, X.S. Direct α-selective glycosylations of acetyl-protected 2-deoxy- and 2,6-dideoxythioglycosides by preactivation protocol. Synlett 2010, 1519-1524.
-
Synlett
, vol.2010
, pp. 1519-1524
-
-
Lu, Y.S.1
Li, Q.2
Wang, Y.H.3
Ye, X.S.4
-
76
-
-
0035955202
-
Oxazolidinone protected 2-amino-2-deoxy-d-glucose derivatives as versatile intermediates in stereoselective oligosaccharide synthesis and the formation of α-linked glycosides
-
Benakli, K.; Zha, C.; Kerns, R.J. Oxazolidinone protected 2-amino-2-deoxy-d-glucose derivatives as versatile intermediates in stereoselective oligosaccharide synthesis and the formation of α- linked glycosides. J. Am. Chem. Soc. 2001, 123, 9461-9462.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 9461-9462
-
-
Benakli, K.1
Zha, C.2
Kerns, R.J.3
-
77
-
-
21844445623
-
Ethyl 2-acetamido-4,6-di-O-benzyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β- D-glycopyranoside as a versatile GlcNAc donor
-
Boysen, M.; Gemma, E.; Lahmann, M.; Oscarson, S. Ethyl 2-acetamido-4,6-di-O-benzyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D- glycopyranoside as a versatile GlcNAc donor. Chem. Commun. 2005, 3044-3046.
-
(2005)
Chem. Commun.
, pp. 3044-3046
-
-
Boysen, M.1
Gemma, E.2
Lahmann, M.3
Oscarson, S.4
-
78
-
-
0141459399
-
Extended applications and potential limitations of ring-fused 2,3-oxazolidinone thioglycosides in glycoconjugate synthesis
-
Kerns, R.J.; Zha, C.X.; Benakli, K.; Liang, Y.Z. Extended applications and potential limitations of ring-fused 2,3-oxazolidinone thioglycosides in glycoconjugate synthesis. Tetrahedron Lett. 2003, 44, 8069-8072.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 8069-8072
-
-
Kerns, R.J.1
Zha, C.X.2
Benakli, K.3
Liang, Y.Z.4
-
79
-
-
18744406719
-
Factors affecting stereocontrol during glycosidation of 2,3-oxazolidinone-protected 1-tolylthio-N-acetyl-D-glucosamine
-
Wei, P.; Kerns, R.J. Factors affecting stereocontrol during glycosidation of 2,3-oxazolidinone-protected 1-tolylthio-N-acetyl-D-glucosamine. J. Org. Chem. 2005, 70, 4195-4198.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 4195-4198
-
-
Wei, P.1
Kerns, R.J.2
-
80
-
-
38349084460
-
Pre-activation protocol leading to highly stereoselectivity-controllable glycosylations of oxazolidinone protected glucosamines
-
Geng, Y.Q.; Zhang, L.H.; Ye, X.S. Pre-activation protocol leading to highly stereoselectivity-controllable glycosylations of oxazolidinone protected glucosamines. Chem. Commun. 2008, 597-599.
-
(2008)
Chem. Commun.
, pp. 597-599
-
-
Geng, Y.Q.1
Zhang, L.H.2
Ye, X.S.3
-
81
-
-
42749084884
-
Stereoselectivity investigation on glycosylation of oxazolidinone protected 2-amino-2-deoxy-D-glucose donors based on pre-activation protocol
-
Geng, Y.Q.; Zhang, L.H.; Ye, X.S. Stereoselectivity investigation on glycosylation of oxazolidinone protected 2-amino-2-deoxy-D-glucose donors based on pre-activation protocol. Tetrahedron 2008, 64, 4949-4958.
-
(2008)
Tetrahedron
, vol.64
, pp. 4949-4958
-
-
Geng, Y.Q.1
Zhang, L.H.2
Ye, X.S.3
-
82
-
-
52449124502
-
Investigations of glycosylation reactions with 2-N-acetyl-2N,3-O- oxazolidinone-protected glucosamine donors
-
Olsson, J.D.M.; Eriksson, L.; Lahmann, M.; Oscarson, S. Investigations of glycosylation reactions with 2-N-acetyl-2N,3O-oxazolidinone-protected glucosamine donors. J. Org. Chem. 2008, 73, 7181-7188.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7181-7188
-
-
Olsson, J.D.M.1
Eriksson, L.2
Lahmann, M.3
Oscarson, S.4
-
83
-
-
77955656016
-
A highly α-selective glycosylation for the convenient synthesis of repeating α-(1→4)-linked N-acetyl-galactosamine units
-
Yang, L.; Ye, X.S. A highly α-selective glycosylation for the convenient synthesis of repeating α-(1→4)-linked N-acetyl- galactosamine units. Carbohydr. Res. 2010, 345, 1713-1721.
-
(2010)
Carbohydr. Res.
, vol.345
, pp. 1713-1721
-
-
Yang, L.1
Ye, X.S.2
-
84
-
-
33747799654
-
N-Benzyl-2,3-oxazolidinone as a glycosyl donor for selective α-glycosylation and one-pot oligosaccharide synthesis involving 1,2-cis-glycosylation
-
Manabe, S.; Ishii, K.; Ito, Y. N-Benzyl-2,3-oxazolidinone as a glycosyl donor for selective α-glycosylation and one-pot oligosaccharide synthesis involving 1,2-cis-glycosylation. J. Am. Chem. Soc. 2006, 128, 10666-10667.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10666-10667
-
-
Manabe, S.1
Ishii, K.2
Ito, Y.3
-
85
-
-
33744918059
-
Stereoselective synthesis of oligo-α-(2,8)-sialic acids
-
Tanaka, H.; Nishiura, Y.; Takahashi, T. Stereoselective synthesis of oligo-α-(2,8)-sialic acids. J. Am. Chem. Soc. 2006, 128, 7124-7125.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 7124-7125
-
-
Tanaka, H.1
Nishiura, Y.2
Takahashi, T.3
-
86
-
-
66249115290
-
Stereoselective synthesis of α(2,9) di- to tetrasialic acids using a 5,4-N,O-carbonyl protected thiosialoside
-
Tanaka, H.; Nishiura, Y.; Takahashi, T. Stereoselective synthesis of α(2,9) di- to tetrasialic acids, using a 5,4-N,O-carbonyl protected thiosialoside. J. Org. Chem. 2009, 74, 4383-4386.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 4383-4386
-
-
Tanaka, H.1
Nishiura, Y.2
Takahashi, T.3
-
87
-
-
34047235444
-
O-Sialylation with N-acetyl-5-N,4-O-carbonyl-protected thiosialoside donors in dichloromethane: Facile and selective cleavage of the oxazolidinone ring
-
Crich, D.; Li, W. O-Sialylation with N-acetyl-5-N,4-O-carbonyl-protected thiosialoside donors in dichloromethane: facile and selective cleavage of the oxazolidinone ring. J. Org. Chem. 2007, 72, 2387-2391.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 2387-2391
-
-
Crich, D.1
Li, W.2
-
88
-
-
68949086206
-
Silylene/oxazolidinone double-locked sialic acid building blocks for efficient sialylation reactions in dichloromethane
-
Hanashima, S.; Sato, K.; Ito, Y.; Yamaguchi, Y. Silylene/oxazolidinone double-locked sialic acid building blocks for efficient sialylation reactions in dichloromethane. Eur. J. Org. Chem. 2009, 4215-4220.
-
(2009)
Eur. J. Org. Chem.
, pp. 4215-4220
-
-
Hanashima, S.1
Sato, K.2
Ito, Y.3
Yamaguchi, Y.4
-
89
-
-
0042159799
-
Extending the possibility of an N-Troc-protected sialic acid donor toward variant sialo-glycoside synthesis
-
Ando, H.; Koike, Y.; Ishida, H.; Kiso, M. Extending the possibility of an N-Troc-protected sialic acid donor toward variant sialo-glycoside synthesis. Tetrahedron Lett. 2003, 44, 6883-6886.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6883-6886
-
-
Ando, H.1
Koike, Y.2
Ishida, H.3
Kiso, M.4
-
90
-
-
1642338668
-
An effective sialylation method using N-Troc- and N-Fmoc-protected β-thiophenyl sialosides and application to the one-pot two-step synthesis of 2,6-sialyl-T antigen
-
Adachi, M., Tanaka, H.; Takahashi, T. An effective sialylation method using N-Troc- and N-Fmoc- protected β-thiophenyl sialosides and application to the one-pot two-step synthesis of 2,6-sialyl-T antigen. Synlett 2004, 609-614.
-
(2004)
Synlett
, pp. 609-614
-
-
Adachi, M.1
Tanaka, H.2
Takahashi, T.3
-
91
-
-
0042671098
-
Di-tert-butylsilylene (DTBS) group-directed α-selective galactosylation unaffected by C-2 participating functionalities
-
Imamura, A.; Ando, H.; Korogi, S.; Tanabe, G.; Muraoka, O.; Ishida, H.; Kiso, M. Di-tert-butylsilylene (DTBS) group-directed α-selective galactosylation unaffected by C-2 participating functionalities. Tetrahedron Lett. 2003, 44, 6725-6728.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6725-6728
-
-
Imamura, A.1
Ando, H.2
Korogi, S.3
Tanabe, G.4
Muraoka, O.5
Ishida, H.6
Kiso, M.7
-
92
-
-
33845212293
-
Extended applications of di-tert-butylsilylene-directed α-predominant galactosylation compatible with C2-participating groups toward the assembly of various glycosides
-
Imamura, A.; Kimura, A.; Ando, H.; Ishida, H.; Kiso, M. Extended applications of di-tert-butylsilylene-directed α-predominant galactosylation compatible with C2-participating groups toward the assembly of various glycosides. Chem. Eur. J. 2006, 12, 8862-8870.
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 8862-8870
-
-
Imamura, A.1
Kimura, A.2
Ando, H.3
Ishida, H.4
Kiso, M.5
-
93
-
-
0000023645
-
Experimental and theoretical evidence of through-space electrostatic stabilization of the incipient oxocarbenium ion by an axially oriented electronegative substituent during glycopyranoside acetolysis
-
Miljkovic, M.; Yeagley, D.; Deslongchamps, P.; Dory, Y. Experimental and theoretical evidence of through-space electrostatic stabilization of the incipient oxocarbenium ion by an axially oriented electronegative substituent during glycopyranoside acetolysis. J. Org. Chem. 1997, 62, 7597-7604.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7597-7604
-
-
Miljkovic, M.1
Yeagley, D.2
Deslongchamps, P.3
Dory, Y.4
-
94
-
-
47249092878
-
DTBS (di-tert-butylsilylene)-directed α-galactosylation for the synthesis of biologically relevant glycans
-
Imamura, A.; Ando, H.; Ishida, H.; Kiso, M. DTBS (di-tert-butylsilylene)- directed α-galactosylation for the synthesis of biologically relevant glycans. Curr. Org. Chem. 2008, 12, 675-689.
-
(2008)
Curr. Org. Chem.
, vol.12
, pp. 675-689
-
-
Imamura, A.1
Ando, H.2
Ishida, H.3
Kiso, M.4
-
95
-
-
52549133610
-
Design and efficient synthesis of novel GM2 analogues with respect to the elucidation of the function of GM2 activator
-
Komori, T.; Ando, T.; Imamura, A.; Li, Y.T.; Ishida, H.; Kiso, M. Design and efficient synthesis of novel GM2 analogues with respect to the elucidation of the function of GM2 activator. Glycoconjugate J. 2008, 25, 647-661.
-
(2008)
Glycoconjugate J.
, vol.25
, pp. 647-661
-
-
Komori, T.1
Ando, T.2
Imamura, A.3
Li, Y.T.4
Ishida, H.5
Kiso, M.6
-
96
-
-
33748513467
-
Practical approach for the stereoselective introduction of β-arabinofuranosides
-
Zhu, X.; Kawatkar, S.; Rao, Y.; Boons, G. Practical approach for the stereoselective introduction of β-arabinofuranosides. J. Am. Chem. Soc. 2006, 128, 11948-11957.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 11948-11957
-
-
Zhu, X.1
Kawatkar, S.2
Rao, Y.3
Boons, G.4
-
97
-
-
0037427286
-
2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages
-
Gadikota, R.R.; Callam, C.S.; Wagner, T.; Del Fraino, B.; Lowary, T.L. 2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages. J. Am. Chem. Soc. 2003, 125, 4155-4165.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 4155-4165
-
-
Gadikota, R.R.1
Callam, C.S.2
Wagner, T.3
Del Fraino, B.4
Lowary, T.L.5
-
98
-
-
34547916785
-
Synthesis of the docosanasaccharide arabinan domain of mycobacterial arabinogalactan and a proposed octadecasaccharide biosynthetic precursor
-
Joe, M.; Bai, Y.; Nacario, R.C.; Lowary, T.L. Synthesis of the docosanasaccharide arabinan domain of mycobacterial arabinogalactan and a proposed octadecasaccharide biosynthetic precursor. J. Am. Chem. Soc. 2007, 129, 9885-9901.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 9885-9901
-
-
Joe, M.1
Bai, Y.2
Nacario, R.C.3
Lowary, T.L.4
-
99
-
-
33846003822
-
Stereoselective synthesis of a fragment of mycobacterial arabinan
-
Ishiwata, A.; Akao, H.; Ito, Y. Stereoselective synthesis of a fragment of mycobacterial arabinan. Org. Lett. 2006, 8, 5525-5528.
-
(2006)
Org. Lett.
, vol.8
, pp. 5525-5528
-
-
Ishiwata, A.1
Akao, H.2
Ito, Y.3
-
100
-
-
33644980281
-
Synthesis and TNF-α inducing activities of mycoloyl-arabinan motif of mycobacterial cell wall components
-
Ishiwata, A.; Akao, H.; Ito, Y.; Sunagawa, M.; Kusunose, N.; Kashiwazaki, Y. Synthesis and TNF-α inducing activities of mycoloyl-arabinan motif of mycobacterial cell wall components. Bioorg. Med. Chem. 2006, 14, 3049-3061.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 3049-3061
-
-
Ishiwata, A.1
Akao, H.2
Ito, Y.3
Sunagawa, M.4
Kusunose, N.5
Kashiwazaki, Y.6
-
101
-
-
0242414726
-
Nucleophilic additions to fused bicyclic five-membered ring oxocarbenium ions: Evidence for preferential attack on the inside face
-
Smith, D.M.; Tran, M.B.; Woerpel, K.A. Nucleophilic additions to fused bicyclic five-membered ring oxocarbenium ions: evidence for preferential attack on the inside face. J. Am. Chem. Soc. 2003, 125, 14149-14152.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 14149-14152
-
-
Smith, D.M.1
Tran, M.B.2
Woerpel, K.A.3
-
102
-
-
34247582306
-
β-Selective glucosylation in the absence of neighboring group participation: Influence of the 3,4-O-bisacetal protecting system
-
Crich, D.; Subramanian, V.; Hutton, T.K. β-Selective glucosylation in the absence of neighboring group participation: influence of the 3,4-O-bisacetal protecting system. Tetrahedron 2007, 63, 5042-5049.
-
(2007)
Tetrahedron
, vol.63
, pp. 5042-5049
-
-
Crich, D.1
Subramanian, V.2
Hutton, T.K.3
-
103
-
-
77955679176
-
β-Selective arabinofuranosylation using a 2,3-O-xylylene-protected donor
-
Imamura, A.; Lowary, T.L. β-Selective arabinofuranosylation using a 2,3-O-xylylene-protected donor. Org. Lett. 2010, 12, 3686-3689.
-
(2010)
Org. Lett.
, vol.12
, pp. 3686-3689
-
-
Imamura, A.1
Lowary, T.L.2
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