-
1
-
-
37049097827
-
α-C-Glycopyranosides from Lewis Acid Catalysed Condensations of Acetylated Glycals and Enol Silanes
-
Dawe, R. D.; Fraser-Raid, B. α-C-Glycopyranosides from Lewis Acid Catalysed Condensations of Acetylated Glycals and Enol Silanes. J. Chem. Soc., Chem. Commun. 1981, 1180-1181.
-
(1981)
J. Chem. Soc., Chem. Commun.
, pp. 1180-1181
-
-
Dawe, R.D.1
Fraser-Raid, B.2
-
2
-
-
20944434408
-
Ultrasound in Organic Synthesis. 2. Formation and Reaction of Organocopper Reagents
-
Danishefsky, S. J.; Kerwin, J. F. Jr. Ultrasound in Organic Synthesis. 2. Formation and Reaction of Organocopper Reagents. J. Org. Chem. 1982, 47, 3805-3806.
-
(1982)
J. Org. Chem.
, vol.47
, pp. 3805-3806
-
-
Danishefsky, S.J.1
Kerwin Jr., J.F.2
-
3
-
-
37049103130
-
Activation of 6-endo over 5-exo Epoxide Openings. Ring-selective Formation of Tetrahydropyran Systems and Stereocontrolled Synthesis of the ABC Ring Framework of Brevetoxin B
-
Nicolaou, K. C.; Duggan, M. E.; Hwang, C.-K.; Somers, P. K. Activation of 6-endo over 5-exo Epoxide Openings. Ring-selective Formation of Tetrahydropyran Systems and Stereocontrolled Synthesis of the ABC Ring Framework of Brevetoxin B. J. Chem. Soc., Chem. Commun. 1985, 1359-1362.
-
(1985)
J. Chem. Soc. Chem. Commun.
, pp. 1359-1362
-
-
Nicolaou, K.C.1
Duggan, M.E.2
Hwang, C.-K.3
Somers, P.K.4
-
4
-
-
84961346861
-
Iterative Assembly of Glycols and Glycal Derivatives: The synthesis of Glycosylated Natural Products and Complex Oligosaccharides
-
Ernst, B., Hart, G. W., Sinay, P., Eds.; Wiley-VCH Verlag GmbH: Weinheim, Germany Chapter 3
-
Williams, L. J.; Garbaccio, R. M.; Danishefsky, S. J. Iterative Assembly of Glycols and Glycal Derivatives: The synthesis of Glycosylated Natural Products and Complex Oligosaccharides. In Carbohydrates in Chemistry and Biology; Ernst, B., Hart, G. W., Sinay, P., Eds.; Wiley-VCH Verlag GmbH: Weinheim, Germany, 2000; Volume 1, Chapter 3, pp. 61-92.
-
(2000)
Carbohydrates in Chemistry and Biology
, vol.1
, pp. 61-92
-
-
Williams, L.J.1
Garbaccio, R.M.2
Danishefsky, S.J.3
-
5
-
-
0000328143
-
Solid-Phase Synthesis of Oligosaccharides and Glycoconjugates by the Glycal Assembly Method: A Five Year Retrospective
-
Seeberger, P. H.; Danishefsky, S. J. Solid-Phase Synthesis of Oligosaccharides and Glycoconjugates by the Glycal Assembly Method: A Five Year Retrospective. Acc. Chem. Res. 1998, 31, 685-695.
-
(1998)
Acc. Chem. Res.
, vol.31
, pp. 685-695
-
-
Seeberger, P.H.1
Danishefsky, S.J.2
-
6
-
-
0030989756
-
Monitoring the Progress of Solid-Phase Oligosaccharide Synthesis by High-Resolution Magic Angle Spinning NMR: Observations of Enhanced Selectivity for β-Glycoside Formation from α-1,2-Anhydrosugar Donors in Solid-Phase Couplings
-
Seeberger, P. H.; Beebe, X.; Sukenick, G. D.; Pochapsky, S.; Danishefsky, S. J. Monitoring the Progress of Solid-Phase Oligosaccharide Synthesis by High-Resolution Magic Angle Spinning NMR: Observations of Enhanced Selectivity for β-Glycoside Formation from α-1,2-Anhydrosugar Donors in Solid-Phase Couplings. Angew. Chem. Int. Ed. 1997, 36, 491-493.
-
(1997)
Angew. Chem. Int. Ed.
, vol.36
, pp. 491-493
-
-
Seeberger, P.H.1
Beebe, X.2
Sukenick, G.D.3
Pochapsky, S.4
Danishefsky, S.J.5
-
8
-
-
0001207175
-
Solid Support Oligosaccharide Synthesis: Construction of β-Linked Oligosaccharides by Coupling of Glycal Derived Thioethyl Glycosyl Donors
-
Zheng, C.; Seeberger, P. H.; Danishefsky, S. J. Solid Support Oligosaccharide Synthesis: Construction of β-Linked Oligosaccharides by Coupling of Glycal Derived Thioethyl Glycosyl Donors. J. Org. Chem. 1998, 63, 1126-1130.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1126-1130
-
-
Zheng, C.1
Seeberger, P.H.2
Danishefsky, S.J.3
-
9
-
-
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
-
10
-
-
0001823520
-
Unsaturated Carbohydrates. Part II. Three Reactions Leading to Unsaturated Glycopyranosides
-
(a)
-
(a) Ferrier, R. J. Unsaturated Carbohydrates. Part II. Three Reactions Leading to Unsaturated Glycopyranosides. J. Chem. Soc. 1964, 5443-5449.
-
(1964)
J. Chem. Soc.
, pp. 5443-5449
-
-
Ferrier, R.J.1
-
11
-
-
37049123760
-
Unsaturated Carbohydrates Part IV. Allylic Rearrangement Reactions of 3,4,6-Tri-O-acetyl-D-galactal
-
(b) (C)
-
(b) Ciment, D. M.; Ferrier, R. J. Unsaturated Carbohydrates Part IV. Allylic Rearrangement Reactions of 3,4,6-Tri-O-acetyl-D-galactal. J. Chem. Soc. (C) 1966, 441-445.
-
(1966)
J. Chem. Soc.
, pp. 441-445
-
-
Ciment, D.M.1
Ferrier, R.J.2
-
12
-
-
0001283316
-
Stereochemical Consequences of the Lewis Acid Catalyzed Cyclocondensation of Oxygenated Dienes with Aldehydes. A Rapid and Stereoselective Entry to Various Natural Products Derived from Propionate
-
Danishefsky, S.; Kato, N.; Askin, D.; Kerwin, Jr. J. F. Stereochemical Consequences of the Lewis Acid Catalyzed Cyclocondensation of Oxygenated Dienes with Aldehydes. A Rapid and Stereoselective Entry to Various Natural Products Derived from Propionate. J. Am. Chem. Soc. 1982, 104, 360-362.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 360-362
-
-
Danishefsky, S.1
Kato, N.2
Askin, D.3
Kerwin Jr., J.F.4
-
13
-
-
0026511348
-
Pyranose α-Enones Provided Ready Access to Functionalized trans-Decalins via Bis-annulated Pyranosides Obtained by Intramolecular Diels-Alder Reactions. A Key Intermediate for Forskolin
-
Tsang, R.; Fraser-Reid, B, Pyranose α-Enones Provided Ready Access to Functionalized trans-Decalins via Bis-annulated Pyranosides Obtained by Intramolecular Diels-Alder Reactions. A Key Intermediate for Forskolin. J. Org. Chem. 1992, 57, 1065-1067.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 1065-1067
-
-
Tsang, R.1
Fraser-Reid, B.2
-
14
-
-
0000918324
-
Intramolecular Radical Cyclizations of 2-Deoxy-2-iodohexopyranoside Derivatives: Routes to Densely Functionalized Carbocycles
-
(a)
-
(a) Vite, G. D.; Alonso, R.; Fraser-Reid, B. Intramolecular Radical Cyclizations of 2-Deoxy-2-iodohexopyranoside Derivatives: Routes to Densely Functionalized Carbocycles. J. Org. Chem. 1989, 54, 2268-2271.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 2268-2271
-
-
Vite, G.D.1
Alonso, R.2
Fraser-Reid, B.3
-
15
-
-
0028096635
-
Free Radical Methodology for Carbohydrate to Carbocycle Transformations: An Efficient Synthesis of the Tricyclic Dihydrofuran Portion of Azadirachtin
-
(b)
-
(b) Henry, K. J.; Fraser-Reid, B. Free Radical Methodology for Carbohydrate to Carbocycle Transformations: An Efficient Synthesis of the Tricyclic Dihydrofuran Portion of Azadirachtin. J. Org. Chem. 1994, 59, 5128-5129.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 5128-5129
-
-
Henry, K.J.1
Fraser-Reid, B.2
-
16
-
-
0028018510
-
A Divergent Route for a Total Synthesis of Cyclophellitol and Epicyclophellitol from a [2.2.2]-Oxabicyclic Glycoside Prepared from D-Glucal
-
(a)
-
(a) McDevitt, R. E.; Fraser-Reid, B. A Divergent Route for a Total Synthesis of Cyclophellitol and Epicyclophellitol from a [2.2.2]-Oxabicyclic Glycoside Prepared from D-Glucal. J. Org. Chem. 1994, 59, 3250-3252.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 3250-3252
-
-
McDevitt, R.E.1
Fraser-Reid, B.2
-
17
-
-
0001946536
-
Some Progeny of 2,3-Unsaturated Sugars: They Little Resemble Grandfather Glucose: Twenty Years Later
-
(b)
-
(b) Fraser-Reid, B. Some Progeny of 2,3-Unsaturated Sugars: They Little Resemble Grandfather Glucose: Twenty Years Later. Acc. Chem. Res. 1996, 29, 57-66.
-
(1996)
Acc. Chem. Res.
, vol.29
, pp. 57-66
-
-
Fraser-Reid, B.1
-
18
-
-
0942277393
-
Synthesis and Uses of exo-Glycals
-
Tailefumier, C.; Chapleur, Y. Synthesis and Uses of exo-Glycals. Chem. Rev. 2004, 104, 263-292.
-
(2004)
Chem. Rev.
, vol.104
, pp. 263-292
-
-
Tailefumier, C.1
Chapleur, Y.2
-
19
-
-
0034620905
-
The Expeditious Preparation and Reactivity of Some Protected Forms of Gluconolactone
-
Yang, W.-B.; Tsai, C.-H.; Lin, C.-H. The Expeditious Preparation and Reactivity of Some Protected Forms of Gluconolactone. Tetrahedron Lett. 2000, 41, 2569-2572.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 2569-2572
-
-
Yang, W.-B.1
Tsai, C.-H.2
Lin, C.-H.3
-
20
-
-
33845554860
-
Highly Stereoselective Approaches to α- and β-C-Glycopyranosides
-
Lewis, M. D.; Cha, J. K.; Kishi, Y. Highly Stereoselective Approaches to α- and β-C-Glycopyranosides. J. Am. Chem. Soc. 1982, 104, 4467-4978.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 4467-4978
-
-
Lewis, M.D.1
Cha, J.K.2
Kishi, Y.3
-
21
-
-
0035833085
-
Expeditious Synthesis of C-Glycosyl Conjugated Dienes and Aldehydes from Sugar Lactones
-
Yang, W.-B.; Chang, C.-F.; Wang, S.-H.; Teo, C.-F.; Lin, C.-H. Expeditious Synthesis of C-Glycosyl Conjugated Dienes and Aldehydes from Sugar Lactones. Tetrahedron Lett. 2001, 42, 4657-4660.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4657-4660
-
-
Yang, W.-B.1
Chang, C.-F.2
Wang, S.-H.3
Teo, C.-F.4
Lin, C.-H.5
-
22
-
-
0035944178
-
Facile Synthesis of Conjugated exo-Glycals
-
Yang, W.-B.; Wu, C.-Y.; Chang, C.-C.; Wang, S.-H.; Teo, C.-F.; Lin, C.-H. Facile Synthesis of Conjugated exo-Glycals. Tetrahedron Lett. 2001, 42, 6907-6910.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 6907-6910
-
-
Yang, W.-B.1
Wu, C.-Y.2
Chang, C.-C.3
Wang, S.-H.4
Teo, C.-F.5
Lin, C.-H.6
-
23
-
-
0037204706
-
Stereochemistry in the Synthesis and Reaction of exo-Glycals
-
Yang, W.-B.; Yang, Y.-Y.; Gu, Y.-F.; Wang, S.-H.; Chang, C.-C.; Lin, C.-H. Stereochemistry in the Synthesis and Reaction of exo-Glycals. J. Org. Chem. 2002, 67, 3773-3782.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3773-3782
-
-
Yang, W.-B.1
Yang, Y.-Y.2
Gu, Y.-F.3
Wang, S.-H.4
Chang, C.-C.5
Lin, C.-H.6
-
24
-
-
0001177640
-
Palladium-catalyzed 1,3-Oxygen-to-Carbon Alkyl Shifts. A Cyclopentanone Synthesis
-
Trost, B. M.; Runge, T. A. Palladium-catalyzed 1,3-Oxygen-to-Carbon Alkyl Shifts. A Cyclopentanone Synthesis. J. Am. Chem. Soc. 1981, 103, 7559-7572.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 7559-7572
-
-
Trost, B.M.1
Runge, T.A.2
-
25
-
-
0942293010
-
Reactions of Ynamines with Esters, γ-Butyrolactones and δ-Valerolactones
-
Ficini, J.; Genet, J. P.; Depezay, J. C. Reactions of Ynamines with Esters, γ-Butyrolactones and δ-Valerolactones. Bull. Soc. Chim. Fr. 1973, 12, Pt. 2, 3367-3368.
-
(1973)
Bull. Soc. Chim. Fr.
, vol.12
, Issue.PART 2
, pp. 3367-3368
-
-
Ficini, J.1
Genet, J.P.2
Depezay, J.C.3
-
26
-
-
0025959623
-
Methylenation of Aldonolactones
-
Csuk, R.; Glänzer, B. I. Methylenation of Aldonolactones. Tetrahedron 1991, 47, 1655-1664.
-
(1991)
Tetrahedron
, vol.47
, pp. 1655-1664
-
-
Csuk, R.1
Glänzer, B.I.2
-
27
-
-
0000269618
-
Dichloromethylenation of Lactones. 6. Efficient Synthesis of Dichloroolefins from Lactones and Acetates Using Triphenylphosphine and Tetrachloromethane
-
Lakhrissi, M.; Chapleur, Y. Dichloromethylenation of Lactones. 6. Efficient Synthesis of Dichloroolefins from Lactones and Acetates Using Triphenylphosphine and Tetrachloromethane. J. Org. Chem. 1994, 59, 5752-5757.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 5752-5757
-
-
Lakhrissi, M.1
Chapleur, Y.2
-
28
-
-
84982373258
-
Tertiary Phosphane/Tetrachloromethane, a Versatile Reagent for Chlorination, Dehydration, and P-N Linkage Angew
-
(a)
-
(a) Appel, R. Tertiary Phosphane/Tetrachloromethane, a Versatile Reagent for Chlorination, Dehydration, and P-N Linkage Angew. Chem. Int. Ed. 1975, 14, 801-811.
-
(1975)
Chem. Int. Ed.
, vol.14
, pp. 801-811
-
-
Appel, R.1
-
29
-
-
0013631266
-
Acetonitrile: An Excellent Solvent for the 1,1-Dichloromethylenation of Certain Ketones
-
(b)
-
(b) Burton, G.; Elder, J. S.; Fell, S. C. M.; Stachulski, A.V. Acetonitrile: An Excellent Solvent for the 1,1-Dichloromethylenation of Certain Ketones. Tetrahedron Lett. 1988, 29, 3003-3006.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 3003-3006
-
-
Burton, G.1
Elder, J.S.2
Fell, S.C.M.3
Stachulski, A.V.4
-
31
-
-
0032497604
-
Stereocontrolled Synthesis of β-C-Glycosides and Amino β-C-Glycosides by Wittig Olefination of Perbenzylated Glyconolactones Derivatives
-
Molina, A.; Czernecki, S.; Xie, J. Stereocontrolled Synthesis of β-C-Glycosides and Amino β-C-Glycosides by Wittig Olefination of Perbenzylated Glyconolactones Derivatives. Tetrahedron Lett. 1998, 39, 7507-7510.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 7507-7510
-
-
Molina, A.1
Czernecki, S.2
Xie, J.3
-
32
-
-
0033411661
-
Alkylidenation of Sugar Lactones and Further Transformation to C-Glycosides
-
Xie, J. Molina, A.; Czernecki, S. Alkylidenation of Sugar Lactones and Further Transformation to C-Glycosides. J. Carbohydr. Chem. 1999, 18, 481-498.
-
(1999)
J. Carbohydr. Chem.
, vol.18
, pp. 481-498
-
-
Xie, J.1
Molina, A.2
Czernecki, S.3
-
33
-
-
0029967484
-
Mitsunobu-type Alkylation with Active Methine Compounds
-
Tsunoda, T.; Nagino, C.; Oguri, M.; Ito, S. Mitsunobu-type Alkylation with Active Methine Compounds. Tetrahedron Lett. 1996, 37, 2459-2462.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 2459-2462
-
-
Tsunoda, T.1
Nagino, C.2
Oguri, M.3
Ito, S.4
-
34
-
-
0034635618
-
Efficient Conditions for the Synthesis of C-Glycosylidene Derivatives: A Direct and Stereoselective Route to C-Glycosyl Compounds
-
Lakhrissi, Y.; Taillefumier, C.; Lakhrissi, M.; Chapleur, Y. Efficient Conditions for the Synthesis of C-Glycosylidene Derivatives: A Direct and Stereoselective Route to C-Glycosyl Compounds. Tetrahedron: Asymm. 2000, 11, 417-421.
-
(2000)
Tetrahedron: Asymm.
, vol.11
, pp. 417-421
-
-
Lakhrissi, Y.1
Taillefumier, C.2
Lakhrissi, M.3
Chapleur, Y.4
-
35
-
-
0034620209
-
Cyanomethylene-trimethylphosphorane, A Powerful Reagent for the Wittig Olefination of Esters, Lactones and Imides
-
Tsunoda, T.; Takagi, H.; Takaba, D.; Kaku, H.; Ito, S. Cyanomethylene-trimethylphosphorane, A Powerful Reagent for the Wittig Olefination of Esters, Lactones and Imides. Tetrahedron Lett. 2000, 41, 235-237.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 235-237
-
-
Tsunoda, T.1
Takagi, H.2
Takaba, D.3
Kaku, H.4
Ito, S.5
-
36
-
-
0001849763
-
The Conversion of 2,6-Anhydro-1-deoxy-D-galacto-hept-1-enitol into 1-Deoxy-D-galacto-heptulose by β-D-Galactosidase
-
Brockhaus, M.: Lehmann, J. The Conversion of 2,6-Anhydro-1-deoxy-D-galacto-hept-1-enitol into 1-Deoxy-D-galacto-heptulose by β-D-Galactosidase. Carbohydr. Res. 1977, 53, 21-31.
-
(1977)
Carbohydr. Res.
, vol.53
, pp. 21-31
-
-
Brockhaus, M.1
Lehmann, J.2
-
38
-
-
37049109868
-
Synthesis of C-Glycosyl Compounds. Part 2. Reactions of Aldonic Acid Lactones with Ethyl Isocyanoacetate
-
Hall, R. H.; Bischofberger, K. Eitelman, S. J.; Jordaan, A. Synthesis of C-Glycosyl Compounds. Part 2. Reactions of Aldonic Acid Lactones with Ethyl Isocyanoacetate. J. Chem. Soc., Perkin Trans. 1 1977, 2236-2241.
-
(1977)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 2236-2241
-
-
Hall, R.H.1
Bischofberger, K.2
Eitelman, S.J.3
Jordaan, A.4
-
39
-
-
0002640160
-
Diastereotopic Substrates of β-D-Galactosidase from Escherichia coli as Probes for a Catalytically Active, Protonating Group
-
Fritz, H.; Lehmann, J.; Schlesselmann, P. Diastereotopic Substrates of β-D-Galactosidase from Escherichia coli as Probes for a Catalytically Active, Protonating Group. Carbohydr. Res. 1983, 113, 71-92.
-
(1983)
Carbohydr. Res.
, vol.113
, pp. 71-92
-
-
Fritz, H.1
Lehmann, J.2
Schlesselmann, P.3
-
40
-
-
0942271242
-
Chain Elongation by a Seemingly Stereo-specific Cyanohydrin Synthesis: The Preparation and Configurational Assignment of 3,7-Anhydro-D-threo-L-talo-and -D-galacto-octose
-
Fritz, H.; Lehmann, J.; Schlesselmann, P. Chain Elongation by a Seemingly Stereo-specific Cyanohydrin Synthesis: the Preparation and Configurational Assignment of 3,7-Anhydro-D-threo-L-talo-and -D-galacto-octose. Carbohydr. Res. 1979, 74, 309-318.
-
(1979)
Carbohydr. Res.
, vol.74
, pp. 309-318
-
-
Fritz, H.1
Lehmann, J.2
Schlesselmann, P.3
-
41
-
-
0024197159
-
Synthesis of (Z)-3,7-Anhydro-1,2-dideoxy-2-deuterio-D-gluco-oct-2-enitol, a Prochiral Substrate for Probing the Catalytic Functioning of Glucosylases
-
Weiser, W.; Lehmann, J.; Brewer, C. F.; Hehre, E. J. Synthesis of (Z)-3,7-Anhydro-1,2-dideoxy-2-deuterio-D-gluco-oct-2-enitol, a Prochiral Substrate for Probing the Catalytic Functioning of Glucosylases. Carbohdr. Res. 1988, 183, 287-299.
-
(1988)
Carbohdr. Res.
, vol.183
, pp. 287-299
-
-
Weiser, W.1
Lehmann, J.2
Brewer, C.F.3
Hehre, E.J.4
-
42
-
-
0001533568
-
The Base-induced Rearrangement of α-Halo Sulfones
-
Paquette, L. A. The Base-induced Rearrangement of α-Halo Sulfones. Acc. Chem. Res. 1968, 1, 209-216
-
(1968)
Acc. Chem. Res.
, vol.1
, pp. 209-216
-
-
Paquette, L.A.1
-
43
-
-
0000578851
-
Are Nucleophilic Bimolecular Concerted Reactions Involving Four or More Bonds a Myth?
-
Bordwell, F. G. Are Nucleophilic Bimolecular Concerted Reactions Involving Four or More Bonds a Myth? Acc. Chem, Res. 1970, 3, 281-290.
-
(1970)
Acc. Chem, Res.
, vol.3
, pp. 281-290
-
-
Bordwell, F.G.1
-
44
-
-
0032578741
-
A Ramberg-Bäcklund Approach to exo-Glycals
-
Griffin, F. K.; Murphy, P. V.; Paterson, D. E.; Taylor, R. J. K. A Ramberg-Bäcklund Approach to exo-Glycals. Tetrahedron Lett. 1998, 39, 8179-8182.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8179-8182
-
-
Griffin, F.K.1
Murphy, P.V.2
Paterson, D.E.3
Taylor, R.J.K.4
-
45
-
-
0032487986
-
Benzylic C-glycosides via the Ramberg-Bäcklund Reaction
-
Belica, P. S.; Franck, R. W. Benzylic C-glycosides via the Ramberg-Bäcklund Reaction. Tetrahedron Lett. 1998, 39, 8225-8228
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8225-8228
-
-
Belica, P.S.1
Franck, R.W.2
-
46
-
-
0032578809
-
Synthetic Applications of Ramberg-Bäcklund Derived exo-Glycals
-
Alcaraz, M.-L., Griffin, F. K.; Paterson, D. E.; Taylor, R. J. K. Synthetic Applications of Ramberg-Bäcklund Derived exo-Glycals. Tetrahedron Lett. 1998, 39, 8183-8186.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8183-8186
-
-
Alcaraz, M.-L.1
Griffin, F.K.2
Paterson, D.E.3
Taylor, R.J.K.4
-
47
-
-
0036204489
-
A Ramberg- Bäcklund Approach to the Synthesis of C-Glycosides, C-Linked Disaccharides, and C-Glycosyl Amino Acids
-
Paterson, D. E.; Griffin, F. K.; Alcaraz, M.-L.; Taylor, R. J. K. A Ramberg- Bäcklund Approach to the Synthesis of C-Glycosides, C-Linked Disaccharides, and C-Glycosyl Amino Acids. Eur. J. Org. 2002, 1323-1336.
-
(2002)
Eur. J. Org.
, pp. 1323-1336
-
-
Paterson, D.E.1
Griffin, F.K.2
Alcaraz, M.-L.3
Taylor, R.J.K.4
-
48
-
-
0035945770
-
Synthesis and Growth Inhibitory Properties of Glucosamine-derived Glycerolipids
-
Yang, G.; Franck, R. W.; Bittman, R.; Samadder, P.; Arthur, G. Synthesis and Growth Inhibitory Properties of Glucosamine-derived Glycerolipids. Org. Lett. 2001, 3, 197-200.
-
(2001)
Org. Lett.
, vol.3
, pp. 197-200
-
-
Yang, G.1
Franck, R.W.2
Bittman, R.3
Samadder, P.4
Arthur, G.5
-
49
-
-
0030710083
-
A Stereocontrolled Radical Access to C-Allyl β-D-Glycopyranosides from Glycopyranosylidene Dihalides found en route to C-Glycodienes
-
Praly, J.-P.; Chen, G.-R.; Gola, J.; Hetzer, G.; Raphoz, C. A Stereocontrolled Radical Access to C-Allyl β-D-Glycopyranosides from Glycopyranosylidene Dihalides found en route to C-Glycodienes. Tetrahedron Lett. 1997, 38, 8185-8188.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8185-8188
-
-
Praly, J.-P.1
Chen, G.-R.2
Gola, J.3
Hetzer, G.4
Raphoz, C.5
-
50
-
-
0036218393
-
A New Route to exo-Glycals Using the Ramberg- Bäcklund Rearrangenmet
-
Griffin, F. K.; Paterson, D. E.; Murphy, P. V.; Taylor, R. J. K. A New Route to exo-Glycals Using the Ramberg- Bäcklund Rearrangenmet. Eur. J. Org. 2002, 1305-13226.
-
(2002)
Eur. J. Org.
, pp. 1305-13226
-
-
Griffin, F.K.1
Paterson, D.E.2
Murphy, P.V.3
Taylor, R.J.K.4
-
51
-
-
29444452361
-
A similar trend was reported in the studies of enol ethers
-
3rd Ed. Springer Verlag: Berlin
-
A similar trend was reported in the studies of enol ethers. Pretsch, E.; Bühlmann, P,; Affolter, C. In Structural Determination of Organic Compounds, 3rd Ed. Springer Verlag: Berlin, 2000, p. 172.
-
(2000)
Structural Determination of Organic Compounds
, pp. 172
-
-
Pretsch, E.1
Bühlmann, P.2
Affolter, C.3
-
52
-
-
0001909281
-
Dichloromethylenation of 1,4-lactones. A New Access to 1-Deoxy-1-C-methyl-C-glycosyl Compounds
-
Bandzouzi, A.; Chapleur, Y. Dichloromethylenation of 1,4-lactones. A New Access to 1-Deoxy-1-C-methyl-C-glycosyl Compounds. Carbohydr. Res. 1987, 171, 13-24.
-
(1987)
Carbohydr. Res.
, vol.171
, pp. 13-24
-
-
Bandzouzi, A.1
Chapleur, Y.2
-
53
-
-
0034635618
-
Efficient Conditions for the Synthesis of C-Glycosylidene Derivatives: A Direct and Stereoselective Route to C-Glycosyl Compounds
-
Lakhrissi, Y.; Taillefumier, C.; Lakhrissi, M.; Chapleur, Y. Efficient Conditions for the Synthesis of C-Glycosylidene Derivatives: A Direct and Stereoselective Route to C-Glycosyl Compounds. Tetrahedron: Asymmetry 2000, 11, 417-421.
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 417-421
-
-
Lakhrissi, Y.1
Taillefumier, C.2
Lakhrissi, M.3
Chapleur, Y.4
-
54
-
-
0032487986
-
Benzylic C-Glycosides via the Ramberg-Bäcklund Reaction
-
Belica, P. S.; Franck, R. W. Benzylic C-Glycosides via the Ramberg-Bäcklund Reaction. Tetrahedron Lett. 1998, 39, 8225-8228.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8225-8228
-
-
Belica, P.S.1
Franck, R.W.2
-
55
-
-
37049071511
-
Dichloromethylenation of Sugar γ-Lactones: A Stereospecific Synthesis of L-(+)-Muscarine and L-(+)-Epimuscarine Toluene-p-Sulphonates
-
Bandzouzi, A.; Chapleur, Y. Dichloromethylenation of Sugar γ-Lactones: A Stereospecific Synthesis of L-(+)-Muscarine and L-(+)-Epimuscarine Toluene-p-Sulphonates. J. Chem. Soc. Perkin Trans. 1 1987, 661-664.
-
(1987)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 661-664
-
-
Bandzouzi, A.1
Chapleur, Y.2
-
56
-
-
37049109647
-
A Convenient Synthesis of Substituted Chiral Tetrahydrofurans from Sugar γ-lactones
-
Chapleur, Y. A Convenient Synthesis of Substituted Chiral Tetrahydrofurans from Sugar γ-lactones. J. Chem. Soc. Chem. Commun. 1984, 449-450.
-
(1984)
J. Chem. Soc. Chem. Commun.
, pp. 449-450
-
-
Chapleur, Y.1
-
57
-
-
0034649190
-
Synthesis of (+)-Muscarine from (S)-(-)-5-Hydroxymethyl-2(5H)-furanone
-
Kang, K. H.; Cha, M. Y.; Pae, A. N.; Choi, K. I.; Cho, Y. S.; Koh, H. Y.; Chung, B. Y. Synthesis of (+)-Muscarine from (S)-(-)-5-Hydroxymethyl-2(5H)-furanone. Tetrahedron Lett. 2000, 41, 8137-8140.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 8137-8140
-
-
Kang, K.H.1
Cha, M.Y.2
Pae, A.N.3
Choi, K.I.4
Cho, Y.S.5
Koh, H.Y.6
Chung, B.Y.7
-
58
-
-
0037041234
-
Stereoselective Synthesis of a C-Glycoside Analog of N-Fmoc-Serine β-N-Acetylglucosaminide by Ramberg-Bäcklund Rearrangement
-
Ohnishi, Y.; Ichikawa, Y. Stereoselective Synthesis of a C-Glycoside Analog of N-Fmoc-Serine β-N-Acetylglucosaminide by Ramberg-Bäcklund Rearrangement. Bioorg. Med. Chem. Lett. 2002, 12, 997-999.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 997-999
-
-
Ohnishi, Y.1
Ichikawa, Y.2
-
59
-
-
0000846840
-
1-Methylene sugars as C-Glycoside Precursors
-
RajanBabu, T. V.; Reddy, G. S. 1-Methylene sugars as C-Glycoside Precursors. J. Org. Chem. 1986, 51, 5458-5461.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 5458-5461
-
-
RajanBabu, T.V.1
Reddy, G.S.2
-
60
-
-
0034693096
-
C-Glycoside Based Mimics of D-myo-Inositol 1,4,5-Trisphosphate
-
Rosenberg, H. J.; Riley, A. M.; Correa, V.; Taylor, C. W.; Potter, B. V. C-Glycoside Based Mimics of D-myo-Inositol 1,4,5-Trisphosphate. Carbohydr. Res. 2000, 329, 7-16.
-
(2000)
Carbohydr. Res.
, vol.329
, pp. 7-16
-
-
Rosenberg, H.J.1
Riley, A.M.2
Correa, V.3
Taylor, C.W.4
Potter, B.V.5
-
61
-
-
0034043542
-
Carbohydrate-Based Mimics of D-myo-Inositol 1,4,5-Trisphosphate
-
Chretien, F.; Moitessier, N.; Roussel, F.; Manger, J.-P.; Chapleur, Y. Carbohydrate-Based Mimics of D-myo-Inositol 1,4,5-Trisphosphate. Curr. Org. Chem. 2000, 4, 513-534.
-
(2000)
Curr. Org. Chem.
, vol.4
, pp. 513-534
-
-
Chretien, F.1
Moitessier, N.2
Roussel, F.3
Manger, J.-P.4
Chapleur, Y.5
-
62
-
-
0028205619
-
Two-step Stereoselective Conversion of 5-Monosubstituted 1,3-Dioxolan-4-ones into Selectively Protected 2,3 -Erythro-1,2,3-triols. A Route to Polyhydroxylated Molecules
-
Untersteller, E.; Xin, Y. C.; Sinaÿ, P. Two-step Stereoselective Conversion of 5-Monosubstituted 1,3-Dioxolan-4-ones into Selectively Protected 2,3 -Erythro-1,2,3-triols. A Route to Polyhydroxylated Molecules. Tetrahedron Lett. 1994, 35, 2537-2540.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 2537-2540
-
-
Untersteller, E.1
Xin, Y.C.2
Sinaÿ, P.3
-
63
-
-
0032481078
-
New Strategy for Convergent Synthesis of trans-Fused Polyether Frameworks Based on Palladium-catalyzed Suzuki Cross-coupling Reaction
-
Sasaki, M.; Fuwa, H.; Inoue, M.; Tachibana, K. New Strategy for Convergent Synthesis of trans-Fused Polyether Frameworks Based on Palladium-catalyzed Suzuki Cross-coupling Reaction. Tetrahedron Lett. 1998, 39, 9027-9030.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9027-9030
-
-
Sasaki, M.1
Fuwa, H.2
Inoue, M.3
Tachibana, K.4
-
64
-
-
0033592061
-
exo-Glycal Approaches to C-Linked Glycosyl Amino Acid Synthesis
-
Campbell, A. D.; Paterson, D. E.; Taylor, R. J. K.; Raynham, T. M. exo-Glycal Approaches to C-Linked Glycosyl Amino Acid Synthesis. Chem. Commun. 1999, 1599.
-
Chem. Commun.
, vol.1999
, pp. 1599
-
-
Campbell, A.D.1
Paterson, D.E.2
Taylor, R.J.K.3
Raynham, T.M.4
-
65
-
-
0030952760
-
Synthesis and Biological Evaluation of Aza-C-Disaccharides: (1→6), (1→4), and (1→1)-Linked Sugar Mimics
-
Johns, B. A.; Pan, Y. T.; Elbein, A. D.; Johnson, C. R. Synthesis and Biological Evaluation of Aza-C-Disaccharides: (1→6), (1→4), and (1→1)-Linked Sugar Mimics. J. Am. Chem. Soc. 1997, 119, 4856-4865.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 4856-4865
-
-
Johns, B.A.1
Pan, Y.T.2
Elbein, A.D.3
Johnson, C.R.4
-
66
-
-
0028143277
-
Synthesis of Aza-C-Disaccharides: A New Class of Sugar Mimics
-
Johnson, C. R.; Miller, M. W.; Golebiowski, A.; Sundram, H.; Ksebati, M. B. Synthesis of Aza-C-Disaccharides: A New Class of Sugar Mimics. Tetrahedron Lett. 1994, 35, 8991-8994.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 8991-8994
-
-
Johnson, C.R.1
Miller, M.W.2
Golebiowski, A.3
Sundram, H.4
Ksebati, M.B.5
-
67
-
-
0037048491
-
Inter- and Intramolecular Alcohol additions of exo-Glycals
-
Chang, C.-F., Yang, W.-B., Chang, C.-C.; Lin, C.-H, Inter- and Intramolecular Alcohol additions of exo-Glycals, Tetrahedron Lett. 2002, 43, 6515-6519.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 6515-6519
-
-
Chang, C.-F.1
Yang, W.-B.2
Chang, C.-C.3
Lin, C.-H.4
-
68
-
-
0028114980
-
The Synthesis of Difluoromethylene-linked C-Glycosides and C-Disaccharides
-
Herpin, T. F.; Motherwell, W. B.; Tozer, M. J. The Synthesis of Difluoromethylene-linked C-Glycosides and C-Disaccharides. Tetrahedron: Asymm. 1994, 5, 2269-2282.
-
(1994)
Tetrahedron: Asymm.
, vol.5
, pp. 2269-2282
-
-
Herpin, T.F.1
Motherwell, W.B.2
Tozer, M.J.3
-
69
-
-
85033649267
-
Some Radical Reactions of Exocyclic Carbohydrate Difluoroenol Ethers
-
Motherwell, W. B.; Ross, B. C.; Tozer, M. J. Some Radical Reactions of Exocyclic Carbohydrate Difluoroenol Ethers. Synlett 1989, 68-70.
-
(1989)
Synlett
, pp. 68-70
-
-
Motherwell, W.B.1
Ross, B.C.2
Tozer, M.J.3
-
70
-
-
0000188554
-
Cyclization of Hydroxy Enol Ethers: A Stereocontrolled Approach to 3-Deoxy-D-manno-2-octulosonic Acid Containing Disaccharides
-
Haudrechy, A.; Sinaÿ, P. Cyclization of Hydroxy Enol Ethers: A Stereocontrolled Approach to 3-Deoxy-D-manno-2-octulosonic Acid Containing Disaccharides. J. Org. Chem. 1992, 57, 4142-4151.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 4142-4151
-
-
Haudrechy, A.1
Sinaÿ, P.2
-
71
-
-
0001432336
-
The Synthesis of β-D-Glucopyranosyl 2-Deoxy-α-D-arabino-hexopyranoside
-
(a)
-
(a) Lemieux, R. U.; Morgan, A. R. The Synthesis of β-D-Glucopyranosyl 2-Deoxy-α-D-arabino-hexopyranoside. Can. J. Chem. 1965, 43, 2190-2198.
-
(1965)
Can. J. Chem.
, vol.43
, pp. 2190-2198
-
-
Lemieux, R.U.1
Morgan, A.R.2
-
72
-
-
33845184246
-
On the Controlled Oxidative Coupling of Glycals: A New Strategy for the Rapid Assembly of Oligosaccharides
-
(b)
-
(b) Friesen, R. W.; Danishefsky, S. J. On the Controlled Oxidative Coupling of Glycals: A New Strategy for the Rapid Assembly of Oligosaccharides. J. Am. Chem. Soc. 1989, 111, 6656-6660.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 6656-6660
-
-
Friesen, R.W.1
Danishefsky, S.J.2
-
73
-
-
84987569497
-
Iodonium Ion Promoted Reactions at the Anomeric C-2 Center of 1-Methylene Sugars
-
(c)
-
(c) Noort, D.; Veeneman, G. H.; Boons, G. J. P. H.; van der Marel, G. A.; Mulder, G. J.; van Boom, J. H. Iodonium Ion Promoted Reactions at the Anomeric C-2 Center of 1-Methylene Sugars. Synlett 1990, 205-206.
-
(1990)
Synlett
, pp. 205-206
-
-
Noort, D.1
Veeneman, G.H.2
Boons, G.J.P.H.3
van der Marel, G.A.4
Mulder, G.J.5
van Boom, J.H.6
-
74
-
-
0031592605
-
C-Disaccharides I. Stereoselective approach to β-(1-4)-3-Deoxy-C-Disaccharides from Levoglucosenone
-
Witczak, Z. J.; Chhabra, R.; Chojnacki, J. C-Disaccharides I. Stereoselective approach to β-(1-4)-3-Deoxy-C-Disaccharides from Levoglucosenone. Tetrahedron Lett. 1997, 38, 2215-2218.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 2215-2218
-
-
Witczak, Z.J.1
Chhabra, R.2
Chojnacki, J.3
-
75
-
-
0037666003
-
A One-Pot Synthesis of β-C-Glucopyranosides from exo-Glucal, p-Tolylsulfenyl Chloride, an α-Methoxyalkene, and an External Nucleophile
-
(a)
-
(a) Liu, H.; Smoliakova, I. P.; Koikov, L. N. A One-Pot Synthesis of β-C-Glucopyranosides from exo-Glucal, p-Tolylsulfenyl Chloride, an α-Methoxyalkene, and an External Nucleophile. Org. Lett. 2002, 4, 3895-3898.
-
(2002)
Org. Lett.
, vol.4
, pp. 3895-3898
-
-
Liu, H.1
Smoliakova, I.P.2
Koikov, L.N.3
-
76
-
-
0034076566
-
Synthesis of C-Glycosylic Compounds Using Three-Membered Cyclic Intermediates
-
(b)
-
(b) Smoliakova, I. P. Synthesis of C-Glycosylic Compounds Using Three-Membered Cyclic Intermediates. Curr. Org. Chem. 2000, 4, 589-608.
-
(2000)
Curr. Org. Chem.
, vol.4
, pp. 589-608
-
-
Smoliakova, I.P.1
-
77
-
-
0033537981
-
Reaction of Vinyl Ethers with ArSCl Adducts of D-Glucal
-
(a)
-
(a) Smoliakova, I. P.; Han, M.; Gong, J.; Caple, R.; Smit, W. A. Reaction of Vinyl Ethers with ArSCl Adducts of D-Glucal. Tetrahedron 1999, 55, 4559-4572.
-
(1999)
Tetrahedron
, vol.55
, pp. 4559-4572
-
-
Smoliakova, I.P.1
Han, M.2
Gong, J.3
Caple, R.4
Smit, W.A.5
-
78
-
-
0035831981
-
Stereoselective synthesis of β-C-D-Glucopyranosides Using the Reaction of TMSCN and Grignard Reagents with Cyclic Five-membered Sulfonium Salt Intermediates
-
(b)
-
(b) Liu, H.; Smoliakova, I. P. Stereoselective synthesis of β-C-D-Glucopyranosides Using the Reaction of TMSCN and Grignard Reagents with Cyclic Five-membered Sulfonium Salt Intermediates. Tetrahedron 2001, 57, 2973-2980.
-
(2001)
Tetrahedron
, vol.57
, pp. 2973-2980
-
-
Liu, H.1
Smoliakova, I.P.2
-
79
-
-
0041728893
-
Stereoselective Glycosylation of exo-Glycals Accelerated by Ferrier-type Rearrangement
-
Yang, W.-B.; Lin, H.-C.; Gu, Y.-F.; Chen, C.-Y.; Wu, C.-Y.; Chang, C.-C.; Lin, C.-H. Stereoselective Glycosylation of exo-Glycals Accelerated by Ferrier-type Rearrangement. Org. Lett. 2003, 5, 1087-1089.
-
(2003)
Org. Lett.
, vol.5
, pp. 1087-1089
-
-
Yang, W.-B.1
Lin, H.-C.2
Gu, Y.-F.3
Chen, C.-Y.4
Wu, C.-Y.5
Chang, C.-C.6
Lin, C.-H.7
-
80
-
-
12944304629
-
Streoselective Glycosylation of exo-Glyeals by Microwave-assisted Ferrier Rearrangement
-
Lin, H.-C.; Chang, C.-C.; Chen, J.-Y.; Lin, C.-H. Streoselective Glycosylation of exo-Glyeals by Microwave-assisted Ferrier Rearrangement. Tetrahedron: Asymm. 2005, 16, 297-301.
-
(2005)
Tetrahedron: Asymm.
, vol.16
, pp. 297-301
-
-
Lin, H.-C.1
Chang, C.-C.2
Chen, J.-Y.3
Lin, C.-H.4
-
81
-
-
20544450144
-
Different Reaction Routes Found in Acid-Catalyzed Glycosylation of endo- and exo-Glycals: Competition between Ferrier Rearrangement and Protonation
-
Lin, H.-C.; Du, W.-P.; Chang, C.-C.; Lin, C.-H. Different Reaction Routes Found in Acid-Catalyzed Glycosylation of endo- and exo-Glycals: Competition between Ferrier Rearrangement and Protonation. Tetrahedron Lett. 2005, 46, 5071-5076.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 5071-5076
-
-
Lin, H.-C.1
Du, W.-P.2
Chang, C.-C.3
Lin, C.-H.4
-
82
-
-
0035858616
-
An Efficient Synthesis of New 1′-C- -Methyl-α-O-disaccharides Using 1-Methylenesugars as the Glycosyl Donors
-
(a)
-
(a) Li, X; Ohtake, H.; Takahashi, H.; Ikegami, S. An Efficient Synthesis of New 1′-C- -Methyl-α-O-disaccharides Using 1-Methylenesugars as the Glycosyl Donors. Tetrahedron 2001, 57, 4283-4295.
-
(2001)
Tetrahedron
, vol.57
, pp. 4283-4295
-
-
Li, X.1
Ohtake, H.2
Takahashi, H.3
Ikegami, S.4
-
83
-
-
0035211616
-
Direct Methylenation of Partially Benzyl-Protected Sugar Lactones by Dimethyltitanocene
-
(b)
-
(b) Li, X.; Ohtake, H.; Takahashi, H.; Ikegami, S. Direct Methylenation of Partially Benzyl-Protected Sugar Lactones by Dimethyltitanocene. Synlett 2001, 1885-1888.
-
(2001)
Synlett
, pp. 1885-1888
-
-
Li, X.1
Ohtake, H.2
Takahashi, H.3
Ikegami, S.4
-
84
-
-
15944393889
-
Synthesis of PI-88 Analogue Using Novel O-Glycosidation of exo-Methylenesugars
-
Namme, R.; Mitsugi, T.; Takahashi, H.; Ikegami, S. Synthesis of PI-88 Analogue Using Novel O-Glycosidation of exo-Methylenesugars. Tetrahedron Lett. 2005, 46, 3033-3036.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 3033-3036
-
-
Namme, R.1
Mitsugi, T.2
Takahashi, H.3
Ikegami, S.4
-
85
-
-
0033548699
-
A novel Donor for Stereoselective α-Sialylation; Efficient Synthesis of an α(2-8)-Linked Bis-sialic Acid Unit
-
(a)
-
(a) Hossain, N.; Magnusson, G. A novel Donor for Stereoselective α-Sialylation; Efficient Synthesis of an α(2-8)-Linked Bis-sialic Acid Unit. Tetrahedron Lett. 1999, 40, 2217.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 2217
-
-
Hossain, N.1
Magnusson, G.2
-
86
-
-
0001434616
-
-
(b)
-
(b) Hori, H.; Nakajima, T.; Nishida, Y.; Ohrui, H.; Meguro H. Tetrahedron Lett. 1988, 29, 6317-6320.
-
(1988)
Tetrahedron Lett.
, vol.29
, pp. 6317-6320
-
-
Hori, H.1
Nakajima, T.2
Nishida, Y.3
Ohrui, H.4
Meguro, H.5
-
87
-
-
0035822064
-
Conversion of the Carboxy Group of Sialic Acid Donors to a Protected Hydroxymethyl Group Yields an Efficient Reagent for the Synthesis of the Unnatural beta-Linkage
-
(c)
-
(c) Ye, X.-S.; Huang, X.; Wong. C.-H. Conversion of the Carboxy Group of Sialic Acid Donors to a Protected Hydroxymethyl Group Yields an Efficient Reagent for the Synthesis of the Unnatural beta-Linkage. Chem. Commun. 2001, 974-975.
-
(2001)
Chem. Commun.
, pp. 974-975
-
-
Ye, X.-S.1
Huang, X.2
Wong, C.-H.3
-
88
-
-
0030461311
-
New Antitumor Substances, FR901463, FR901464 and FR901465. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Biological Activities
-
Nakajima, H.; Sato, B.; Fujita, T.; Takase, S.; Terano, H.; Okuhara, M. New Antitumor Substances, FR901463, FR901464 and FR901465. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Biological Activities. J. Antibiot. 1996, 49, 1196-1203.
-
(1996)
J. Antibiot.
, vol.49
, pp. 1196-1203
-
-
Nakajima, H.1
Sato, B.2
Fujita, T.3
Takase, S.4
Terano, H.5
Okuhara, M.6
-
89
-
-
0035904404
-
FR901464: Total Synthesis, Proof of Structure, and Evaluation of Synthetic Analogues
-
Thompson, C. F.; Jamison, T. F.; Jacobsen, E. N. FR901464: Total Synthesis, Proof of Structure, and Evaluation of Synthetic Analogues. J. Am. Chem. Soc. 2001, 123, 9974-9983.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 9974-9983
-
-
Thompson, C.F.1
Jamison, T.F.2
Jacobsen, E.N.3
-
90
-
-
0026656836
-
Reveromycins, New Inhibitors of Eukaryotic Cell Growth. I. Producing Organism, Fermentation, Isolation and Physico-chemical Properties
-
(a)
-
(a) Takahashi, H.; Osada, R; Koshino, H.; Kudo, T.; Amano, S.; Shimizu, S.; Yoshihama, M.; Isono, K. Reveromycins, New Inhibitors of Eukaryotic Cell Growth. I. Producing Organism, Fermentation, Isolation and Physico-chemical Properties. J. Antibiol. 1992, 45, 1409-1413.
-
(1992)
J. Antibiol.
, vol.45
, pp. 1409-1413
-
-
Takahashi, H.1
Osada, R.2
Koshino, H.3
Kudo, T.4
Amano, S.5
Shimizu, S.6
Yoshihama, M.7
Isono, K.8
-
91
-
-
0026764947
-
Reveromycins, New Inhibitors of Eukaryotic Cell Growth. III. Structures of Reveromycins A, B, C and D
-
(b)
-
(b) Koshino, H.; Takahashi, H.; Osada, H.; Kiyoshi, I. Reveromycins, New Inhibitors of Eukaryotic Cell Growth. III. Structures of Reveromycins A, B, C and D. J. Antibiot. 1992, 45, 1420-1427.
-
(1992)
J. Antibiot.
, vol.45
, pp. 1420-1427
-
-
Koshino, H.1
Takahashi, H.2
Osada, H.3
Kiyoshi, I.4
-
92
-
-
0030889521
-
Synthetic Studies toward the Reveromycins: Asymmetric Synthesis of the Spiroketal Segment of Reveromycin B
-
McRae, K. J.; Rizzacasa, M. A. Synthetic Studies toward the Reveromycins: Asymmetric Synthesis of the Spiroketal Segment of Reveromycin B. J. Org. Chem. 1997, 62, 1196-1197.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1196-1197
-
-
McRae, K.J.1
Rizzacasa, M.A.2
-
93
-
-
0034703160
-
Synthetic Approach to 3-Deoxy-D-manno-oct-2-ulosonic Acid (Kdo) α-Disaccharides via a Ketene Dithioacetal
-
Młynarski, J.; Banaszek, A. Synthetic Approach to 3-Deoxy-D-manno-oct-2-ulosonic Acid (Kdo) α-Disaccharides via a Ketene Dithioacetal. Tetrahedron: Asymm. 2000, 11, 3737-3746.
-
(2000)
Tetrahedron: Asymm.
, vol.11
, pp. 3737-3746
-
-
Młynarski, J.1
Banaszek, A.2
-
94
-
-
0020265136
-
+, D-Glucose Cotransporter. A Model Study
-
+, D-Glucose Cotransporter. A Model Study. Biochim, Biophys. Acta 1982, 688, 557-571.
-
(1982)
Biochim, Biophys. Acta
, vol.688
, pp. 557-571
-
-
Toggenburger, G.1
Kessler, M.2
Semenza, G.3
-
95
-
-
0032850016
-
+-glucose Cotransporters, May Provide a Novel Approach to Treating Diabetes
-
+-glucose Cotransporters, May Provide a Novel Approach to Treating Diabetes. Diabetes 1999, 48, 1794-1800.
-
(1999)
Diabetes
, vol.48
, pp. 1794-1800
-
-
Oku, A.1
Ueta, K.2
Arakawa, K.3
Ishihara, T.4
Nawano, M.5
Kuronuma, Y.6
Matsumoto, M.7
Saito, A.8
Tsujihara, K.9
Anai, M.10
Asano, T.11
Kanai, Y.12
Endou, H.13
-
96
-
-
0033619999
-
+-Glucose Cotransporter (SGLT) Inhibitors as Antidiabetic Agents. 4. Synthesis and Pharmacological Properties of 4′-Dehydroxyphlorizin Derivatives Substituted on the B
-
(b)
-
+-Glucose Cotransporter (SGLT) Inhibitors as Antidiabetic Agents. 4. Synthesis and Pharmacological Properties of 4′-Dehydroxyphlorizin Derivatives Substituted on the B Ring. J. Med. Chem. 1999, 42, 5311-5324.
-
(1999)
Ring J. Med. Chem.
, vol.42
, pp. 5311-5324
-
-
Tsujihara, K.1
Hongu, M.2
Saito, K.3
Kawanishi, H.4
Kuriyama, K.5
Matsumoto, M.6
Oku, A.7
Ueta, K.8
Tsuda, M.9
Saito, A.10
-
97
-
-
0034716014
-
A Method for Preparing C-Glycosides Related to Phlorizin
-
Link, J. T.; Sorensen, B. K. A Method for Preparing C-Glycosides Related to Phlorizin. Tetrahedron Lett. 2000, 41, 9213-9217.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 9213-9217
-
-
Link, J.T.1
Sorensen, B.K.2
-
98
-
-
0028830031
-
A Concise Route to Enantiomerically Pure 2-Arylcyclohexenones of Relevance to the Pancratistatin Problem
-
Park, T. K.; Danishefsky, S. J. A Concise Route to Enantiomerically Pure 2-Arylcyclohexenones of Relevance to the Pancratistatin Problem. Tetrahedron Lett. 1995, 36, 195-196.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 195-196
-
-
Park, T.K.1
Danishefsky, S.J.2
-
99
-
-
0030969876
-
A New Bromotyrosine Derivative from a Sponge, Aplysinella sp
-
(a)
-
(a) Liu, S.; Fu, X.; Schmitz, F. J.; Kelly-Borges, M. Psammaplysin F, A New Bromotyrosine Derivative from a Sponge, Aplysinella sp. J. Nat. Prod. 1997, 60, 614-615.
-
(1997)
J. Nat. Prod.
, vol.60
, pp. 614-615
-
-
Liu, S.1
Fu, X.2
Schmitz, F.J.3
Kelly-Borges, M.4
Psammaplysin, F.5
-
100
-
-
0033974331
-
New Moloka'iamine Derivatives from an Undescribed Verongid Sponge
-
(b)
-
(b) Lacy, C.; Scheuer, P. J. New Moloka'iamine Derivatives from an Undescribed Verongid Sponge. J. Nat. Prod. 2000, 63, 119-121.
-
(2000)
J. Nat. Prod.
, vol.63
, pp. 119-121
-
-
Lacy, C.1
Scheuer, P.J.2
-
101
-
-
0037467864
-
Nitrile Oxide Cycloadditions to Olefinated Sugars
-
Colinas, P. A.; Jäger, V.; Lieberknecht, A.; Bravo, R. D. Nitrile Oxide Cycloadditions to Olefinated Sugars. Tetrahedron Lett. 2003, 44, 1071-1074.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 1071-1074
-
-
Colinas, P.A.1
Jäger, V.2
Lieberknecht, A.3
Bravo, R.D.4
-
102
-
-
0035813868
-
α(1-3)-Galactosyl- -transferase Inhibition Based on a New Type of Disubstrate Analogue
-
Waldscheck, B.; Streiff, M.; Notz, W.; Kinzy, W.; Schmidt, R. R. α(1-3)-Galactosyl- -transferase Inhibition Based on a New Type of Disubstrate Analogue. Angew. Chem. Int. Ed. 2001, 40, 4007-4011
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 4007-4011
-
-
Waldscheck, B.1
Streiff, M.2
Notz, W.3
Kinzy, W.4
Schmidt, R.R.5
-
103
-
-
0842307444
-
Novel UDP-Glycal Derivatives as Transition State Analogue Inhibitors of UDP-GlcNAc 2-Epimerase
-
Stoltz, F.; Reiner, M.; Blume, A.; Reinter, W.; Schmidt, R. R. Novel UDP-Glycal Derivatives as Transition State Analogue Inhibitors of UDP-GlcNAc 2-Epimerase. J. Org. Chem. 2004, 69, 665-679.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 665-679
-
-
Stoltz, F.1
Reiner, M.2
Blume, A.3
Reinter, W.4
Schmidt, R.R.5
-
104
-
-
2942705936
-
Efficient Synthesis of a Nucleoside-diphospho-exo-glycal Displaying Time-dependent Inactivation of UDP-Galactopyranose Mutase
-
Caravano, A.; Vincent, S. P.; Sinay, P. Efficient Synthesis of a Nucleoside-diphospho-exo-glycal Displaying Time-dependent Inactivation of UDP-Galactopyranose Mutase. Chem. Commun. 2004, 1216-1217.
-
(2004)
Chem. Commun.
, pp. 1216-1217
-
-
Caravano, A.1
Vincent, S.P.2
Sinay, P.3
-
105
-
-
0034971311
-
Cell Wall Core Galactofuran Synthesis Is Essential for Growth of Mycobacteria
-
Pan, F.; Jackson, M.; Ma, Y.; McNeil, M. Cell Wall Core Galactofuran Synthesis Is Essential for Growth of Mycobacteria. J. Bacteriol. 2001, 183, 3991-3998.
-
(2001)
J. Bacteriol.
, vol.183
, pp. 3991-3998
-
-
Pan, F.1
Jackson, M.2
Ma, Y.3
McNeil, M.4
-
106
-
-
0034833650
-
Mechanistic investigation of UDP-galactopyranose mutase from Escherichia coli using 2- and 3-fluorinated UDP-galactofuranose as probes
-
Zhang, Q.; Liu, H.-w. Mechanistic investigation of UDP-galactopyranose mutase from Escherichia coli using 2- and 3-fluorinated UDP-galactofuranose as probes. J. Am. Chem. Soc. 2001, 123, 6756-6766.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 6756-6766
-
-
Zhang, Q.1
Liu, H.-W.2
-
107
-
-
0035842165
-
Synthesis of a Non-charged Analogue of Guanosyldiphosphofucose
-
Carchon, G.; Chrétien, F.; Delannoy, P.; Verbert, A.; Chapleur, Y. Synthesis of a Non-charged Analogue of Guanosyldiphosphofucose. Tetrahedron Lett. 2001, 42, 8821-8824.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8821-8824
-
-
Carchon, G.1
Chrétien, F.2
Delannoy, P.3
Verbert, A.4
Chapleur, Y.5
-
108
-
-
0030776125
-
Studies on the Synthesis of C-Glycoside Sulfones as Potential Glycosyl Transferase Inhibitors
-
Gervay, J.; Flaherty, T. M.; Holmes, D. Studies on the Synthesis of C-Glycoside Sulfones as Potential Glycosyl Transferase Inhibitors. Tetrahedron 1997, 53, 16355-16364.
-
(1997)
Tetrahedron
, vol.53
, pp. 16355-16364
-
-
Gervay, J.1
Flaherty, T.M.2
Holmes, D.3
-
109
-
-
17544404233
-
Synthesis of Monosaccharide-Derived Spirocyclic Cyclopropylamines and Their Evaluation as Glycosidase Inhibitors
-
Blüchel, C.; Ramana, C. V.; Vasella, A. Synthesis of Monosaccharide-Derived Spirocyclic Cyclopropylamines and Their Evaluation as Glycosidase Inhibitors. Helv. Chim. Acta 2003, 86, 2998-3036.
-
(2003)
Helv. Chim. Acta
, vol.86
, pp. 2998-3036
-
-
Blüchel, C.1
Ramana, C.V.2
Vasella, A.3
-
110
-
-
37049122324
-
Synthesis of Glycosyl α-Amino Acids
-
Bischofberger, K.; Hall, R. H.; Jordan, A. Synthesis of Glycosyl α-Amino Acids. J. Chem. Soc., Chem. Commun. 1975, 806.
-
(1975)
J. Chem. Soc., Chem. Commun.
, pp. 806
-
-
Bischofberger, K.1
Hall, R.H.2
Jordan, A.3
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