-
3
-
-
0346116581
-
-
Wiley-VCH: Weinheim
-
(c) Otera, J. Esterification; Wiley-VCH: Weinheim, 2003, 5-266.
-
(2003)
Esterification
, pp. 5-266
-
-
Otera, J.1
-
4
-
-
0034498920
-
Solid-phase oligosaccharide synthesis and combinatorial carbohydrate libraries
-
For recent review articles on oligosaccharide synthesis see: (a) Seeberger, P.H.; Haase, W.C. Solid-phase oligosaccharide synthesis and combinatorial carbohydrate libraries. Chem. Rev. 2000, 100, 4349-4394;
-
(2000)
Chem. Rev.
, vol.100
, pp. 4349-4394
-
-
Seeberger, P.H.1
Haase, W.C.2
-
5
-
-
0034505430
-
Synthesis of complex carbohydrates and glycoconjugates: Enzyme-based and programmable one-pot strategies
-
(b) Koeller, K.M.; Wong, C.-H. Synthesis of complex carbohydrates and glycoconjugates: enzyme-based and programmable one-pot strategies. Chem. Rev. 2000, 100, 4465-4494.
-
(2000)
Chem. Rev.
, vol.100
, pp. 4465-4494
-
-
Koeller, K.M.1
Wong, C.-H.2
-
6
-
-
0017998510
-
4-Dialkylaminopyridines as acylation catalysts
-
Höfle, G.; Steglich, W.; Vorbrüggen, H. 4-Dialkylaminopyridines as acylation catalysts. Angew. Chem. Int. Ed. Engl. 1978, 17, 569-583.
-
(1978)
Angew. Chem. Int. Ed. Engl.
, vol.17
, pp. 569-583
-
-
Höfle, G.1
Steglich, W.2
Vorbrüggen, H.3
-
7
-
-
80051729483
-
Tributylphosphine: A remarkable acylation catalyst
-
Vedejs, E.; Diver, S.T. Tributylphosphine: a remarkable acylation catalyst. J. Am. Chem. Soc. 1993, 115, 3358-3359.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 3358-3359
-
-
Vedejs, E.1
Diver, S.T.2
-
8
-
-
0344950837
-
Superbase-promoted acylation of hindered alcohols
-
D'Sa, B.A.; Verkade, J.G. Superbase-promoted acylation of hindered alcohols. J. Org. Chem. 1996, 61, 2963-2966.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 2963-2966
-
-
D'Sa, B.A.1
Verkade, J.G.2
-
9
-
-
0037765623
-
Dialkyl imidazolium benzoates-roomtemperature ionic liquids useful in the peracetylation and perbenzoylation of simple and sulfated saccharides
-
(a) Murugesan, S.; Karst, N.; Islam, T.; Wiencek, J.M.; Linhardt, R.J. Dialkyl imidazolium benzoates-roomtemperature ionic liquids useful in the peracetylation and perbenzoylation of simple and sulfated saccharides. Synlett 2003, 1283-1286;
-
(2003)
Synlett
, pp. 1283-1286
-
-
Murugesan, S.1
Karst, N.2
Islam, T.3
Wiencek, J.M.4
Linhardt, R.J.5
-
10
-
-
0037035324
-
Rapid, clean, and mild O-acetylation of alcohols and carbohydrates in an ionic liquid
-
(b) Forsyth, S.A.; MacFarlane, D.R.; Thomson, R.J.; von Itzstein, M. Rapid, clean, and mild O-acetylation of alcohols and carbohydrates in an ionic liquid. Chem. Commun. 2002, 714-715.
-
(2002)
Chem. Commun.
, pp. 714-715
-
-
Forsyth, S.A.1
MacFarlane, D.R.2
Thomson, R.J.3
Von Itzstein, M.4
-
11
-
-
2342646700
-
3
-
3. Green Chem. 2004, 6, 191-192.
-
(2004)
Green Chem.
, vol.6
, pp. 191-192
-
-
Bartoli, G.1
Dalpozzo, R.2
De Nino, A.3
Maiuolo, L.4
Nardi, M.5
Procopio, A.6
Tagarelli, A.7
-
13
-
-
0000578180
-
Acetylation of carbohydrates using ferric chloride in acetic anhydride
-
Dasgupta, F.; Singh, P.P.; Srivastava, H.C. Acetylation of carbohydrates using ferric chloride in acetic anhydride. Carbohydr. Res. 1980, 80, 346-349.
-
(1980)
Carbohydr. Res.
, vol.80
, pp. 346-349
-
-
Dasgupta, F.1
Singh, P.P.2
Srivastava, H.C.3
-
14
-
-
18044401091
-
Catalytic nucleophilic acyl substitution of anhydrides by amphoteric vanadyl triflate
-
Chen, C.-T.; Kuo, J.-H.; Li, C.-H.; Barhate, N.B.; Hon, S.-W.; Li, T.-W; Chao, S.-D.; Liu, C.-C.; Li, Y.-C.; Chang, I.-H.; Lin, J.-S.; Liu, C.-J.; Chou, Y.-C. Catalytic nucleophilic acyl substitution of anhydrides by amphoteric vanadyl triflate. Org. Lett. 2001, 3, 3729-3732.
-
(2001)
Org. Lett.
, vol.3
, pp. 3729-3732
-
-
Chen, C.-T.1
Kuo, J.-H.2
Li, C.-H.3
Barhate, N.B.4
Hon, S.-W.5
Li, T.-W.6
Chao, S.-D.7
Liu, C.-C.8
Li, Y.-C.9
Chang, I.-H.10
Lin, J.-S.11
Liu, C.-J.12
Chou, Y.-C.13
-
15
-
-
85011245852
-
Scandium trifluoromethanesulfonate as an extremely active acylation catalyst
-
Ishihara, K.; Kubota, M.; Kurihara, H.; Yamamoto, H.J. Scandium trifluoromethanesulfonate as an extremely active acylation catalyst. J. Am. Chem. Soc. 1995, 117, 4413-4414;
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 4413-4414
-
-
Ishihara, K.1
Kubota, M.2
Kurihara, H.3
Yamamoto, H.J.4
-
16
-
-
0012615648
-
Scandium trifluoromethanesulfonate as an extremely active lewis acid catalyst in acylation of alcohols with acid anhydrides and mixed anhydrides
-
(b) Ishihara, K.; Kubota, M.; Kurihara, H.; Yamamoto, H. Scandium trifluoromethanesulfonate as an extremely active lewis acid catalyst in acylation of alcohols with acid anhydrides and mixed anhydrides. J. Org. Chem. 1996, 61, 4560-4567.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4560-4567
-
-
Ishihara, K.1
Kubota, M.2
Kurihara, H.3
Yamamoto, H.4
-
17
-
-
0142258946
-
2-catalyzed preparation of per-O-acetylated hexopyranoses with stoichiometric acetic anhydride and sequential one-pot anomeric substitution to thioglycosides under solvent-free conditions
-
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. 2003, 68, 8719-8722.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 8719-8722
-
-
Tai, C.-A.1
Kulkarni, S.S.2
Hung, S.-C.3
-
19
-
-
0041666708
-
Perchloric acid adsorbed on silica gel as a new, highly efficient, and versatile catalyst for acetylation of phenols, thiols, alcohols, and amines
-
Chakraborti, A.K.; Gulhane, R. Perchloric acid adsorbed on silica gel as a new, highly efficient, and versatile catalyst for acetylation of phenols, thiols, alcohols, and amines. Chem. Commun. 2003, 1896-1897.
-
(2003)
Chem. Commun.
, pp. 1896-1897
-
-
Chakraborti, A.K.1
Gulhane, R.2
-
20
-
-
0008866853
-
The intermediacy of sulfate esters in sulfuric acid catalyzed acetylation of carbohydrates
-
Hyatt, J.A.; Tindall, G.W. The intermediacy of sulfate esters in sulfuric acid catalyzed acetylation of carbohydrates. Heterocycles 1993, 35, 227-234.
-
(1993)
Heterocycles
, vol.35
, pp. 227-234
-
-
Hyatt, J.A.1
Tindall, G.W.2
-
21
-
-
0032499135
-
Per-O-acetylation of sugars catalysed by montmorillonite K-10
-
Bhaskar, P.M.; Loganathan, D. Per-O-acetylation of sugars catalysed by montmorillonite K-10. Tetrahedron Lett. 1998, 39, 2215-2218.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 2215-2218
-
-
Bhaskar, P.M.1
Loganathan, D.2
-
22
-
-
0032934388
-
H-Beta zeolite as an efficient catalyst for per-O-acetylation of mono- and disaccharides
-
Bhaskar, P.M.; Loganathan, D. H-Beta zeolite as an efficient catalyst for per-O-acetylation of mono- and disaccharides. Synlett 1999, 129-131.
-
(1999)
Synlett
, pp. 129-131
-
-
Bhaskar, P.M.1
Loganathan, D.2
-
23
-
-
0034032134
-
Heterogeneous catalysis in acetylation of alcohols and phenols promoted by zirconium sulfophenyl phosphonate
-
Curini, M.; Epifano, F.; Marcotullio, M.C.; Rosati, O.; Rossi, M. Heterogeneous catalysis in acetylation of alcohols and phenols promoted by zirconium sulfophenyl phosphonate. Synth. Commun. 2000, 30, 1319-1329.
-
(2000)
Synth. Commun.
, vol.30
, pp. 1319-1329
-
-
Curini, M.1
Epifano, F.2
Marcotullio, M.C.3
Rosati, O.4
Rossi, M.5
-
24
-
-
0000466390
-
Iodine: A versatile reagent in carbohydrate chemistry IV. Per-O-acetylation, regioselective acylation and acetolysis
-
(a) Kartha, K.P.R.; Field, R.A. Iodine: a versatile reagent in carbohydrate chemistry IV. Per-O-acetylation, regioselective acylation and acetolysis. Tetrahedron 1997, 53, 11753-11766;
-
(1997)
Tetrahedron
, vol.53
, pp. 11753-11766
-
-
Kartha, K.P.R.1
Field, R.A.2
-
25
-
-
6344293965
-
Streamlined synthesis of per-O-acetylated sugars, glycosyl iodides, or thioglycosides from unprotected reducing sugars
-
(b) Mukhopadhyay, B.; Kartha, K.P.R.; Russell, D.A.; Field, R.A. Streamlined synthesis of per-O-acetylated sugars, glycosyl iodides, or thioglycosides from unprotected reducing sugars. J. Org. Chem. 2004, 69, 7758-7760.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 7758-7760
-
-
Mukhopadhyay, B.1
Kartha, K.P.R.2
Russell, D.A.3
Field, R.A.4
-
27
-
-
4444281057
-
Simple and efficient per-O-acetylation of carbohydrates by lithium perchlorate catalyst
-
and references cited there in
-
Lu, K.-C.; Hsieh, S.-Y.; Patkar, L.N.; Chen, C.-T.; Lin, C.-C. Simple and efficient per-O-acetylation of carbohydrates by lithium perchlorate catalyst. Tetrahedron 2004, 60, 8967-8973, and references cited there in.
-
(2004)
Tetrahedron
, vol.60
, pp. 8967-8973
-
-
Lu, K.-C.1
Hsieh, S.-Y.2
Patkar, L.N.3
Chen, C.-T.4
Lin, C.-C.5
-
28
-
-
0347927248
-
A facile protocol for direct conversion of unprotected sugars into phenyl 4,6-O-benzylidene-per-O-acetylated-1,2- trans-thioglycosides
-
Larsen, K.; Olsen, C.E.; Motawia, M.S. A facile protocol for direct conversion of unprotected sugars into phenyl 4,6-O-benzylidene-per-O-acetylated- 1,2- trans-thioglycosides. Carbohydr. Res. 2003, 338, 199-202.
-
(2003)
Carbohydr. Res.
, vol.338
, pp. 199-202
-
-
Larsen, K.1
Olsen, C.E.2
Motawia, M.S.3
-
29
-
-
0037051601
-
Selective binding of mannose encapsulated gold nanoparticles on type 1 pili in escherichia coli
-
(a) Lin, C.-C.; Yeh, Y.-C.; Yang, C.-Y.; Chen, C.-L.; Chen, G.-F.; Chen, C.-C.; Wu, Y.-C. Selective binding of mannose encapsulated gold nanoparticles on type 1 pili in escherichia coli. J. Am. Chem. Soc. 2002, 124, 3508-3509;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3508-3509
-
-
Lin, C.-C.1
Yeh, Y.-C.2
Yang, C.-Y.3
Chen, C.-L.4
Chen, G.-F.5
Chen, C.-C.6
Wu, Y.-C.7
-
30
-
-
0035815155
-
Solid-phase synthesis of O-linked glycopeptide analogues of enkephalin
-
(b) Mitchell, S.A.; Pratt, M.R.; Hruby, V.J.; Polt, R. Solid-phase synthesis of O-linked glycopeptide analogues of enkephalin. J. Org. Chem. 2001, 66, 2327-2342;
-
(2001)
J. Org. Chem.
, vol.66
, pp. 2327-2342
-
-
Mitchell, S.A.1
Pratt, M.R.2
Hruby, V.J.3
Polt, R.4
-
31
-
-
0028533626
-
Efficient preparation of allyl 2,3,6,2,3,6-hexa-O-benzyl-β-lactoside and its use as a glycosyl acceptor for chain extension at O-4
-
Dasgupta, F.; Anderson, L. Efficient preparation of allyl 2,3,6,2,3,6-hexa-O-benzyl-β-lactoside and its use as a glycosyl acceptor for chain extension at O-4. Carbohydr. Res. 1994, 264, 155-160.
-
(1994)
Carbohydr. Res.
, vol.264
, pp. 155-160
-
-
Dasgupta, F.1
Anderson, L.2
-
32
-
-
0033518559
-
Programmable one-pot oligosaccharide synthesis
-
Zhang, Z.; Ollmann, I.R.; Ye, X.-S.; Wischnat, R.; Baasov, T.; Wong, C.-H. Programmable one-pot oligosaccharide synthesis. J. Am. Chem. Soc. 1999, 121, 734-753.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 734-753
-
-
Zhang, Z.1
Ollmann, I.R.2
Ye, X.-S.3
Wischnat, R.4
Baasov, T.5
Wong, C.-H.6
-
33
-
-
0037071149
-
A method for obtaining equilibrium tautomeric mixtures of reducing sugars via glycosylamines using nonaqueous media
-
Allavudeen, S.S.; Kuberan, B.; Loganathan, D. A method for obtaining equilibrium tautomeric mixtures of reducing sugars via glycosylamines using nonaqueous media. Carbohydr. Res. 2002, 337, 965-968.
-
(2002)
Carbohydr. Res.
, vol.337
, pp. 965-968
-
-
Allavudeen, S.S.1
Kuberan, B.2
Loganathan, D.3
-
34
-
-
0002904931
-
Acetylation of N-acetylneuraminic acid and its methyl ester
-
Marra, A.; Sinaÿ, P. Acetylation of N-acetylneuraminic acid and its methyl ester. Carbohydr. Res. 1989, 190, 317-322.
-
(1989)
Carbohydr. Res.
, vol.190
, pp. 317-322
-
-
Marra, A.1
Sinaÿ, P.2
-
35
-
-
0030915738
-
A search for pyrophosphate mimics for the development of substrates and inhibitors of glycosyltransferases
-
Wang, R.; Steensma, D.H.; Takaoka, Y.; Yun, J.W.; Kajimoto, T.; Wong, C.-H. A search for pyrophosphate mimics for the development of substrates and inhibitors of glycosyltransferases. Bioorg. Med. Chem. 1997, 5, 661-672.
-
(1997)
Bioorg. Med. Chem.
, vol.5
, pp. 661-672
-
-
Wang, R.1
Steensma, D.H.2
Takaoka, Y.3
Yun, J.W.4
Kajimoto, T.5
Wong, C.-H.6
-
36
-
-
0031022634
-
A convenient synthesis of peracetylated glycosyl halides using bismuth(III) halides as catalysts
-
Montero, J.-L.; Winum, J.-Y.; Lrydet, A.; Kamal, M.; Pavia, A.A.; Roque, J.-P. A convenient synthesis of peracetylated glycosyl halides using bismuth(III) halides as catalysts. Carbohydr. Res. 1997, 297, 175-180.
-
(1997)
Carbohydr. Res.
, vol.297
, pp. 175-180
-
-
Montero, J.-L.1
Winum, J.-Y.2
Lrydet, A.3
Kamal, M.4
Pavia, A.A.5
Roque, J.-P.6
-
37
-
-
84986409745
-
1H-NMR-studie der vier unverzweigten peracetylierten β-D-glucopyranosyl-β-gentiobiosen
-
1H-NMR-studie der vier unverzweigten peracetylierten β-D-glucopyranosyl-β-gentiobiosen. Helv. Chim. Acta 1984, 67, 378-385.
-
(1984)
Helv. Chim. Acta
, vol.67
, pp. 378-385
-
-
Von Rychener, M.1
Bigler, P.2
Pfander, H.3
-
38
-
-
21844512723
-
Synthesis of tetrasaccharide repeating unit of the K-antigen from Klebsiella type-16
-
Choudhury, A.K.; Ray, A.K.; Roy, N. Synthesis of tetrasaccharide repeating unit of the K-antigen from Klebsiella type-16. J. Carbohydr. Chem. 1995, 14, 1153-1163.
-
(1995)
J. Carbohydr. Chem.
, vol.14
, pp. 1153-1163
-
-
Choudhury, A.K.1
Ray, A.K.2
Roy, N.3
-
39
-
-
33751157840
-
Glycosyl phosphites as glycosylation reagents: Scope and mechanism
-
Kondo, H.; Aoki, S.; Ichikawa, Y.; Halcomb, R.L.; Ritzen, H.; Wong, C.-H. Glycosyl phosphites as glycosylation reagents: scope and mechanism. J. Org. Chem. 1994, 59, 864-877.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 864-877
-
-
Kondo, H.1
Aoki, S.2
Ichikawa, Y.3
Halcomb, R.L.4
Ritzen, H.5
Wong, C.-H.6
-
40
-
-
4444224109
-
Synthesis of D-glucopyranosyl(1 → 3)-1-thiol-β-glucosamine disaccharide derivative as building block for the synthesis of hyaluronic acid
-
Lin, C.-C.; Hsu, T.-S.; Lu, K.-C.; Huang, I.-T. Synthesis of D-glucopyranosyl(1 → 3)-1-thiol-β-glucosamine disaccharide derivative as building block for the synthesis of hyaluronic acid. J. Chin. Chem. Soc. 2000, 47, 921-928.
-
(2000)
J. Chin. Chem. Soc.
, vol.47
, pp. 921-928
-
-
Lin, C.-C.1
Hsu, T.-S.2
Lu, K.-C.3
Huang, I.-T.4
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