-
1
-
-
0038824103
-
Automated carbohydrate synthesis to drive chemical glycomics
-
Seeberger PH: Automated carbohydrate synthesis to drive chemical glycomics. Chem Commun 2003:1115-1121.
-
(2003)
Chem Commun
, pp. 1115-1121
-
-
Seeberger, P.H.1
-
2
-
-
0036096338
-
Regioselective glycosylations in solution and on soluble and insoluble polymeric supports
-
Geurtsen R, Boons GJ: Regioselective glycosylations in solution and on soluble and insoluble polymeric supports. Eur J Org Chem 2002:1473-1477.
-
(2002)
Eur J Org Chem
, pp. 1473-1477
-
-
Geurtsen, R.1
Boons, G.J.2
-
4
-
-
0002665307
-
Model systems for studying polyvalent carbohydrate interactions
-
Houseman B.T., Mrksich M. Model systems for studying polyvalent carbohydrate interactions. Top Curr Chem. 218:2002;1-44.
-
(2002)
Top Curr Chem
, vol.218
, pp. 1-44
-
-
Houseman, B.T.1
Mrksich, M.2
-
5
-
-
0000856193
-
Artificial multivalent sugar ligands to understand and manipulate carbohydrate-protein interactions
-
Lindhorst T.K. Artificial multivalent sugar ligands to understand and manipulate carbohydrate-protein interactions. Top Curr Chem. 218:2002;201-235.
-
(2002)
Top Curr Chem
, vol.218
, pp. 201-235
-
-
Lindhorst, T.K.1
-
6
-
-
33746976801
-
Recent developments in glycoconjugates
-
Davis B.G. Recent developments in glycoconjugates. J Chem Soc. 1:1999;3215-3237.
-
(1999)
J Chem Soc
, vol.1
, pp. 3215-3237
-
-
Davis, B.G.1
-
7
-
-
0033516491
-
Olefin metathesis by molybdenum imido alkylidene catalysts
-
Schrock R.R. Olefin metathesis by molybdenum imido alkylidene catalysts. Tetrahedron. 55:1999;8141-8153.
-
(1999)
Tetrahedron
, vol.55
, pp. 8141-8153
-
-
Schrock, R.R.1
-
9
-
-
0038215596
-
Recent developments in olefin cross-metathesis
-
Connon S.J., Blechert S. Recent developments in olefin cross-metathesis. Angew Chem Int Ed Engl. 42:2003;1900-1923.
-
(2003)
Angew Chem Int Ed Engl
, vol.42
, pp. 1900-1923
-
-
Connon, S.J.1
Blechert, S.2
-
10
-
-
0344006321
-
Olefin metathesis and beyond
-
Fürstner A. Olefin metathesis and beyond. Angew Chem Int Ed Engl. 39:2000;3012-3043.
-
(2000)
Angew Chem Int Ed Engl
, vol.39
, pp. 3012-3043
-
-
Fürstner, A.1
-
11
-
-
0001311590
-
Ring opening metathesis polymerization
-
Piotti M.E. Ring opening metathesis polymerization. Curr Opin Solid State Mater Sci. 4:1999;539-547.
-
(1999)
Curr Opin Solid State Mater Sci
, vol.4
, pp. 539-547
-
-
Piotti, M.E.1
-
12
-
-
0034616213
-
Recent applications of olefin metathesis and related reactions in carbohydrate chemistry
-
Roy R, Das SK: Recent applications of olefin metathesis and related reactions in carbohydrate chemistry. Chem Commun 2000:519-529.
-
(2000)
Chem Commun
, pp. 519-529
-
-
Roy, R.1
Das, S.K.2
-
13
-
-
0034081275
-
Olefin metathesis in carbohydrate chemistry
-
Jørgensen M., Hadwiger P., Madsen R., Stütz A.E., Wrodnigg T.M. Olefin metathesis in carbohydrate chemistry. Curr Org Chem. 4:2000;565-588.
-
(2000)
Curr Org Chem
, vol.4
, pp. 565-588
-
-
Jørgensen, M.1
Hadwiger, P.2
Madsen, R.3
Stütz, A.E.4
Wrodnigg, T.M.5
-
14
-
-
84902415597
-
Ring-opening metathesis polymerization (ROMP) of norbornene by a group VIII carbene complex in protic media
-
Nguyen S.T., Johnson L.K., Grubbs R.H. Ring-opening metathesis polymerization (ROMP) of norbornene by a group VIII carbene complex in protic media. J Am Chem Soc. 114:1992;3974-3975.
-
(1992)
J Am Chem Soc
, vol.114
, pp. 3974-3975
-
-
Nguyen, S.T.1
Johnson, L.K.2
Grubbs, R.H.3
-
15
-
-
0001339679
-
Synthesis of glycopolymers of controlled molecular weight by ring-opening metathesis polymerization using well-defined functional group tolerant ruthenium carbene catalysts
-
Fraser C., Grubbs R.H. Synthesis of glycopolymers of controlled molecular weight by ring-opening metathesis polymerization using well-defined functional group tolerant ruthenium carbene catalysts. Macromolecules. 28:1995;7248-7255.
-
(1995)
Macromolecules
, vol.28
, pp. 7248-7255
-
-
Fraser, C.1
Grubbs, R.H.2
-
16
-
-
0001526272
-
Preparation of 'sugar-coated' homopolymers and multiblock ROMP copolymers
-
Nomura K., Schrock R.R. Preparation of 'sugar-coated' homopolymers and multiblock ROMP copolymers. Macromolecules. 29:1996;540-545.
-
(1996)
Macromolecules
, vol.29
, pp. 540-545
-
-
Nomura, K.1
Schrock, R.R.2
-
17
-
-
0034104085
-
Synthesis of end-labeled multivalent ligands for exploring cell-surface-receptor-ligand interactions
-
A very elegant synthesis and application of a functionalised, fluorescent glycopolymer with good ligand affinity. This tool is applied for visualisation of carbohydrate-receptor interactions
-
Gordon E.J., Gestwicki J.E., Strong L.E., Kiessling L.L. Synthesis of end-labeled multivalent ligands for exploring cell-surface-receptor-ligand interactions. Chem Biol. 7:2000;9-16 A very elegant synthesis and application of a functionalised, fluorescent glycopolymer with good ligand affinity. This tool is applied for visualisation of carbohydrate-receptor interactions.
-
(2000)
Chem Biol
, vol.7
, pp. 9-16
-
-
Gordon, E.J.1
Gestwicki, J.E.2
Strong, L.E.3
Kiessling, L.L.4
-
18
-
-
0037062901
-
Synthesis and applications of end-labeled neoglycopolymers
-
Owen R.M., Gestwicki J.E., Young T., Kiessling L.L. Synthesis and applications of end-labeled neoglycopolymers. Org Lett. 4:2002;2293-2296.
-
(2002)
Org Lett
, vol.4
, pp. 2293-2296
-
-
Owen, R.M.1
Gestwicki, J.E.2
Young, T.3
Kiessling, L.L.4
-
19
-
-
0038818902
-
Synthesis of a hyaluronan neoglycopolymer by ring-opening metathesis polymerization
-
Iyer S, Rele S, Grasa G, Nolan S, Chaikof EL: Synthesis of a hyaluronan neoglycopolymer by ring-opening metathesis polymerization. Chem Commun 2003:1518-1519.
-
(2003)
Chem Commun
, pp. 1518-1519
-
-
Iyer, S.1
Rele, S.2
Grasa, G.3
Nolan, S.4
Chaikof, E.L.5
-
20
-
-
0035821021
-
Carbohydrate analogue polymers by ring opening metathesis polymerisation (ROMP) and subsequent catalytic dihydroxylation
-
Meier S, Reisinger H, Haag R, Mecking S, Mülhaupt R, Stelzer F: Carbohydrate analogue polymers by ring opening metathesis polymerisation (ROMP) and subsequent catalytic dihydroxylation. Chem Commun 2001:855-856.
-
(2001)
Chem Commun
, pp. 855-856
-
-
Meier, S.1
Reisinger, H.2
Haag, R.3
Mecking, S.4
Mülhaupt, R.5
Stelzer, F.6
-
21
-
-
0034125768
-
Synthesis of 'molecular asterisks' via sequential cross-metathesis, Sonogashira and cyclotrimerization reactions
-
Dominique R, Liu B, Das SK, Roy R: Synthesis of 'molecular asterisks' via sequential cross-metathesis, Sonogashira and cyclotrimerization reactions. Synthesis 2000:862-868.
-
(2000)
Synthesis
, pp. 862-868
-
-
Dominique, R.1
Liu, B.2
Das, S.K.3
Roy, R.4
-
22
-
-
0037074089
-
Stereoselective synthesis of glycoclusters using an olefin metathesis and Sharpless dihydroxylation sequence
-
Elegant use of a sequence of olefin metathesis reactions for the preparation of a mannose cluster
-
Dominique R., Roy R. Stereoselective synthesis of glycoclusters using an olefin metathesis and Sharpless dihydroxylation sequence. Tetrahedron Lett. 43:2002;395-398 Elegant use of a sequence of olefin metathesis reactions for the preparation of a mannose cluster.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 395-398
-
-
Dominique, R.1
Roy, R.2
-
23
-
-
0033597320
-
Cross-metathesis of N-alkenyl peptoids with O- or C-allyl glycosides
-
Hu Y.J., Roy R. Cross-metathesis of N-alkenyl peptoids with O- or C-allyl glycosides. Tetrahedron Lett. 40:1999;3305-3308.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 3305-3308
-
-
Hu, Y.J.1
Roy, R.2
-
24
-
-
0037179181
-
Construction of carbohydrate-based antitumor vaccines: Synthesis of glycosyl amino acids by olefin cross-metathesis
-
Biswas K., Coltart D.M., Danishefsky S.J. Construction of carbohydrate-based antitumor vaccines: synthesis of glycosyl amino acids by olefin cross-metathesis. Tetrahedron Lett. 43:2002;6107-6110.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 6107-6110
-
-
Biswas, K.1
Coltart, D.M.2
Danishefsky, S.J.3
-
25
-
-
0037126261
-
Development of co- and posttranslational synthetic strategies to C-neoglycopeptides
-
This report demonstrates the power of olefin metathesis in conjunction with peptides. It is shown that olefin-containing oligopeptides can be efficiently crosslinked with alkenyl glycosides
-
McGarvey G.J., Benedum T.E., Schmidtmann F.W. Development of co- and posttranslational synthetic strategies to C-neoglycopeptides. Org Lett. 4:2002;3591-3594 This report demonstrates the power of olefin metathesis in conjunction with peptides. It is shown that olefin-containing oligopeptides can be efficiently crosslinked with alkenyl glycosides.
-
(2002)
Org Lett
, vol.4
, pp. 3591-3594
-
-
Mcgarvey, G.J.1
Benedum, T.E.2
Schmidtmann, F.W.3
-
26
-
-
0033135020
-
Design, synthesis and biological evaluation of aryl-substituted sialyl Lewis X mimetics prepared via cross-metathesis of C-fucopeptides
-
Huwe C.M., Woltering T.J., Jiricek J., Weitz-Schmidt G., Wong C.H. Design, synthesis and biological evaluation of aryl-substituted sialyl Lewis X mimetics prepared via cross-metathesis of C-fucopeptides. Bioorg Med Chem. 7:1999;773-788.
-
(1999)
Bioorg Med Chem
, vol.7
, pp. 773-788
-
-
Huwe, C.M.1
Woltering, T.J.2
Jiricek, J.3
Weitz-Schmidt, G.4
Wong, C.H.5
-
27
-
-
0032482544
-
Ring closing metathesis and cross metathesis of carbohydrate derivatives
-
El Sukkari H., Gesson J.P., Renoux B. Ring closing metathesis and cross metathesis of carbohydrate derivatives. Tetrahedron Lett. 39:1998;4043-4046.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4043-4046
-
-
El Sukkari, H.1
Gesson, J.P.2
Renoux, B.3
-
29
-
-
0035990941
-
Saccharide display on microtiter plates
-
Bryan M.C., Plettenburg O., Sears P., Rabuka D., Wacowich-Sgarbi S., Wong C.H. Saccharide display on microtiter plates. Chem Biol. 9:2002;713-720.
-
(2002)
Chem Biol
, vol.9
, pp. 713-720
-
-
Bryan, M.C.1
Plettenburg, O.2
Sears, P.3
Rabuka, D.4
Wacowich-Sgarbi, S.5
Wong, C.H.6
-
30
-
-
0027969033
-
Metathesis of Ω-unsaturated glucosides with chloro-aryloxide complexes of tungsten, as a new way leading to unsaturated bolaamphiphiles
-
Descotes G., Ramza J., Basset J.M., Pagano S. Metathesis of Ω-unsaturated glucosides with chloro-aryloxide complexes of tungsten, as a new way leading to unsaturated bolaamphiphiles. Tetrahedron Lett. 35:1994;7379-7382.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 7379-7382
-
-
Descotes, G.1
Ramza, J.2
Basset, J.M.3
Pagano, S.4
-
31
-
-
0032556498
-
Alkenyl O- and C-glycopyranoside homodimerization by olefin metathesis reaction
-
Dominique R, Das SK, Roy R: Alkenyl O- and C-glycopyranoside homodimerization by olefin metathesis reaction. Chem Commun 1998:2437-2438.
-
(1998)
Chem Commun
, pp. 2437-2438
-
-
Dominique, R.1
Das, S.K.2
Roy, R.3
-
32
-
-
0038206363
-
Synthesis of pseudo-oligosaccharides by a sequence of yne-ene cross metathesis and Diels-Alder reaction
-
Schürer SC, Blechert S: Synthesis of pseudo-oligosaccharides by a sequence of yne-ene cross metathesis and Diels-Alder reaction. Chem Commun 1999:1203-1204.
-
(1999)
Chem Commun
, pp. 1203-1204
-
-
Schürer, S.C.1
Blechert, S.2
-
33
-
-
0037124568
-
First preparation of spacer-linked cyclic neooligoaminodeoxysaccharides
-
A very useful synthetic strategy towards the synthesis of a range of neoglycoconjugates as aminoglycoside analogs
-
Chen G., Kirschning A. First preparation of spacer-linked cyclic neooligoaminodeoxysaccharides. Chemistry. 8:2002;2717-2729 A very useful synthetic strategy towards the synthesis of a range of neoglycoconjugates as aminoglycoside analogs
-
(2002)
Chemistry
, vol.8
, pp. 2717-2729
-
-
Chen, G.1
Kirschning, A.2
-
34
-
-
0141744688
-
General access to iminosugar C-glycoside building blocks by means of cross-metathesis: A gateway to glycoconjugate mimetics
-
Godin G., Compain P., Martin O.R. General access to iminosugar C-glycoside building blocks by means of cross-metathesis: a gateway to glycoconjugate mimetics. Org Lett. 5:2003;3269-3272.
-
(2003)
Org Lett
, vol.5
, pp. 3269-3272
-
-
Godin, G.1
Compain, P.2
Martin, O.R.3
-
35
-
-
0035966230
-
Synthesis of β-galactose-conjugated chlorins derived by enyne metathesis as galectin-specific photosensitizers for photodynamic therapy
-
The strength of this report lies in the demonstration of the efficacy and functional group tolerance of olefin metathesis and its utility in the ligation of highly diverse biomolecules. Furthermore, the products show promise in targeted photodynamic therapy
-
Zheng G., Graham A., Shibata M., Missert J.R., Oseroff A.R., Dougherty T.J., Pandey R.K. Synthesis of β-galactose-conjugated chlorins derived by enyne metathesis as galectin-specific photosensitizers for photodynamic therapy. J Org Chem. 66:2001;8709-8716 The strength of this report lies in the demonstration of the efficacy and functional group tolerance of olefin metathesis and its utility in the ligation of highly diverse biomolecules. Furthermore, the products show promise in targeted photodynamic therapy.
-
(2001)
J Org Chem
, vol.66
, pp. 8709-8716
-
-
Zheng, G.1
Graham, A.2
Shibata, M.3
Missert, J.R.4
Oseroff, A.R.5
Dougherty, T.J.6
Pandey, R.K.7
-
36
-
-
0033518044
-
Solid-phase oligosaccharide synthesis: Preparation of complex structures using a novel linker and different glycosylation agents
-
The design of the solid-phase linker reported here implies that not only the cleavage conditions from the support are orthogonal with most conceivable functional groups, but also that the cleavage products can be used in a further glycosylation reaction. Furthermore, it is demonstrated that complex carbohydrates can be synthesised efficiently using this system
-
Andrade R.B., Plante O.J., Melean L.G., Seeberger P.H. Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylation agents. Org Lett. 1:1999;1811-1814 The design of the solid-phase linker reported here implies that not only the cleavage conditions from the support are orthogonal with most conceivable functional groups, but also that the cleavage products can be used in a further glycosylation reaction. Furthermore, it is demonstrated that complex carbohydrates can be synthesised efficiently using this system.
-
(1999)
Org Lett
, vol.1
, pp. 1811-1814
-
-
Andrade, R.B.1
Plante, O.J.2
Melean, L.G.3
Seeberger, P.H.4
-
37
-
-
0035874702
-
Solution and solid-support synthesis of a potential Leishmaniasis carbohydrate vaccine
-
Hewitt M.C., Seeberger P.H. Solution and solid-support synthesis of a potential Leishmaniasis carbohydrate vaccine. J Org Chem. 66:2001;4233-4243.
-
(2001)
J Org Chem
, vol.66
, pp. 4233-4243
-
-
Hewitt, M.C.1
Seeberger, P.H.2
-
38
-
-
0033867017
-
Solid-phase synthesis of a branched hexasaccharide related to lacto-N-hexaose
-
Knerr L, Schmidt RR: Solid-phase synthesis of a branched hexasaccharide related to lacto-N-hexaose. Eur J Org Chem 2000:2803-2808.
-
(2000)
Eur J Org Chem
, pp. 2803-2808
-
-
Knerr, L.1
Schmidt, R.R.2
-
39
-
-
0032706852
-
Application of a ring closing metathesis based linker to the solid phase synthesis of oligosaccharides
-
Knerr L, Schmidt RR: Application of a ring closing metathesis based linker to the solid phase synthesis of oligosaccharides. Synlett 1999:1802-1804.
-
(1999)
Synlett
, pp. 1802-1804
-
-
Knerr, L.1
Schmidt, R.R.2
-
40
-
-
0032537081
-
Ruthenium-catalyzed yne-ene cross metathesis immobilization of functionalized alkynes
-
Schuster M., Blechert S. Ruthenium-catalyzed yne-ene cross metathesis immobilization of functionalized alkynes. Tetrahedron Lett. 39:1998;2295-2298.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2295-2298
-
-
Schuster, M.1
Blechert, S.2
|