SYNTHESIS OF C-GLYCOSIDES OF BIOLOGICAL INTEREST

[1]  F. Nicotra,et al.  Stereoselective synthesis of the isosteric phosphono analogues of N-acetyl-alpha-D-glucosamine 1-phosphate and N-acetyl-alpha-D-mannosamine 1-phosphate , 1996 .

[2]  F. Nicotra,et al.  Glycomimetics via a new glycoexoenitols–malonyl radical C–C bond formation , 1996 .

[3]  A. Passaniti,et al.  The α-Glucosidase I Inhibitor Castanospermine Alters Endothelial Cell Glycosylation, Prevents Angiogenesis, and Inhibits Tumor Growth , 1995 .

[4]  Chi‐Huey Wong,et al.  Enzymes in Organic Synthesis: Application to the Problems of Carbohydrate Recognition (Part 1) , 1995 .

[5]  M. Benaglia,et al.  Gazz. Chim. Ital , 1995 .

[6]  M. Tozer,et al.  THE SYNTHESIS OF DIFLUOROMETHYLENE-LINKED C-GLYCOSIDES AND C-DISACCHARIDES , 1994 .

[7]  H. Nishino,et al.  Isolation and identification of anti-tumor-promoting principles from the fresh-water cyanobacterium Phormidium tenue. , 1993, Chemical & pharmaceutical bulletin.

[8]  F. Nicotra,et al.  Simple and stereoselective chemoenzymatic synthesis of an α-C-mannoside , 1993 .

[9]  F. Nicotra,et al.  Synthesis of C-disaccharides through dimerization of exo-glycals , 1992 .

[10]  F. Nicotra,et al.  SYNTHETIC STUDIES ON ALPHA-C-GLYCOSIDES OF D-GLUCOSAMINE , 1992 .

[11]  F. Nicotra,et al.  Stereoselective synthesis of the isosteric bisphosphono analogue of β-D-fructose 2,6-bisphosphate , 1990 .

[12]  F. Nicotra,et al.  Synthesis of 1-(α-D-glucopyranosyl)-1-deoxy-D-fructose a non-metabolisable analogue of sucrose , 1989 .

[13]  F. Nicotra,et al.  A new procedure for the synthesis of D-glucosamine α-C-glycosides , 1989 .

[14]  F. Nicotra,et al.  Easy synthesis of a C-disaccharide , 1989 .

[15]  E. Clercq Potential drugs for the treatment of AIDS , 1989 .

[16]  F. Nicotra,et al.  Vinylation-electrophilic cyclization of aldopentoses: easy and stereoselective access to C-glycopyranosides of rare sugars , 1988 .

[17]  Y. Kishi,et al.  Synthesis of C-sucrose , 1988 .

[18]  F. Nicotra,et al.  Synthesis of C-glycosyl compounds by the wittig iodocyclization procedure. Differences from mercuriocyclization , 1987 .

[19]  F. Nicotra,et al.  Stereoselective access to .alpha.- and .beta.-D-fructofuranosyl C-glycosides , 1987 .

[20]  D. Liotta,et al.  Stereoselectivity of electrophile-promoted cyclizations of .gamma.-hydroxyalkenes. An investigation of carbohydrate-derived and model substrates , 1987 .

[21]  G. Gray,et al.  An efficient synthesis of anhydroalditols and allylic-glycosides , 1987 .

[22]  A. Kobata Malignant Transformational Changes of the Sugar Chains of Glycoproteins and Their Clinical Application , 1987 .

[23]  M. Greene,et al.  Development and Recognition of the Transformed Cell , 1987, Springer US.

[24]  F. Lichtenthaler,et al.  A facile access to trisaccharides with central β-D-mannose, α-D-glucosamine, and β-D-mannosamine units , 1985 .

[25]  H. Hers The discovery and the biological role of fructose 2,6-bisphosphate. , 1984, Biochemical Society transactions.

[26]  F. Nicotra,et al.  Synthesis of the phosphono analogues of α- and β-d-mannopyranosyl phosphate , 1984 .

[27]  C. Wilcox,et al.  A new approach to c-glycoside congeners: Metal carbene mediated methylenation of aldonolactones. , 1984 .

[28]  Y. Chapleur A convenient synthesis of substituted chiral tetrahydrofurans from sugar γ-lactones , 1984 .

[29]  F. Nicotra,et al.  High stereoselective synthesis of diethyl (2,3-isopropylidene-5-trityl-α-d-ribofuranosyl)-methanephosphonate, a precursor to the phosphono analog of α-d-ribose 1-phosphate , 1984 .

[30]  F. Nicotra,et al.  Stereospecific synthesis of ethyl (2-acetamido-2-deoxy-α-d-glucopyranosyl)-acetate , 1983 .

[31]  F. Nicotra,et al.  Influence of the protective groups on the ring closure of gluco-octenoates , 1982 .

[32]  F. Nicotra,et al.  Stereospecific synthesis of the phosphono analogs of .alpha.- and .beta.-D-glucose 1-phosphate , 1982 .

[33]  Y. Kishi,et al.  Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosides , 1982 .

[34]  R. Tschesche,et al.  C‐Glycosylflavonoide, I. Synthese von 4′,7‐Di‐O‐methylisobayin [6‐(β‐D‐Glucopyranosyl)‐7‐methoxy‐2‐(4‐methoxyphenyl)‐4H‐1‐benzopyran‐4‐on] , 1982 .

[35]  D. Tulshian,et al.  Stereoselective routes to some unsaturated α- and β-C-glycopyranosides , 1979 .

[36]  J. G. Moffatt,et al.  C-glycosyl nucleosides. V. Some unexpected observations on the relative stabilities of compounds containing fused five-membered rings with epimerizable substituents. , 1975, Journal of the American Chemical Society.

[37]  S. Hanessian,et al.  Facile access to ethyl 2-C-β-D-ribofuranosylacetates , 1974 .

[38]  C. D. Hurd,et al.  Reactions of Polyacylglycosyl Halides with Grignard Reagents , 1950 .

[39]  W. Bonner,et al.  The Glycosylation of Hydrocarbons by Means of the Grignard Reagent , 1945 .