Table Of Content

Carbohydrate Research, 250 (1993) C9-C16 Elsevier Science Publishers B.V., Amsterdam AUTHOR INDEX Alton, G. 145 Kashem, M.A. 129, 145 Amochaeva, V.Y. 211 Kiss, L. 195 Aso, D. 177 Knirel, Y.A. 275 Kocharova, N.A. 275 Baker, D.C. 315 Kochetkov, N.K. 211, 275 Bar-Guilloux, E. 1 Koh, D. 231, 249, 261 Basu, S. 335 Korth, A. 67 BeMiller, J.N. 93, 101 Berger, A. 67 Lai, W. 185 Bernabé, M. 289 Le, N. 87 Bhattacharyya, T. 335 Leal, J.A. 289 Bilik, V. 203 Legler, G. 67, vii Black, T.S. 195 Lehmann, J. 1, 31 Blanchard, J.S. 45 Lemieux, R.U. 87 Bock, K. 87 Liessem, B. 19 Brewer, C.F. 45 Marsano, E. 301 Brovarskaya, O.S. 275 Martin, O.R. 185 Chivers, P.T. 9 Matsui, H. 45 Cosani, A. 301 Matulova, M. 203 Moskalenko, N.V. 275 Defaye, J. 1 Muras, V.A. 275 Dietrich, H. 161 Murata, T. 57 Musser, J.H. Cl Ekhart, C. 67 Myers, R.W. 93, 101 El Sadek, M.M. 323 Nardin, R. 1 El Soccary, N.N. 323 Nashed, M.A. Cl Ermert, P. 113 Nieger, M. 19 Focher, B. 301 Nifant’ev, N.E. 211, 275 Nikrad, P.V. 145 Giannis, A. 19 Ogawa, K. 57 Gilson, R.J. 93, 101 Ogawa, S. 177 Gémez-Miranda, B. 289 Gradnig, G. 67 Padmaperuma, B. 79 Gregson, J.M. 129 Palcic, M.M. 87 Prieto, A. 289 Hehre, E.J. 45 Horton, D. 231, 249, 261 Rob, B. 31 Huber, R.E. 9 Robic, D. 1 Rupitz, K. 113 Jiménez-Barbero, J. 289 Jiricek, R. 31 Sandhoff, K. 19 Johnson, S.C. 315 Santoro, M.M. 93, 101 C10 Author index / Carbohydr. Res. 250 (1993) C9-C10 Scheuring, M. 31 Varbanets, L.D. 275 Schmidt, R.R. 161 Vasella, A. 113 Shashkov, A.S. 211, 275 Venot, A.P. 129, 145 Sinnott, M.L. 79 Skrydstrup, T. 87 Weber, M. 113 Stiitz, A.E. 67 Withers, S.G. 113, 195 Wlasichuk, K.B. 129, 145 Tagliaferri, F. 315 Wu, E. 327 Takagi, Y. 261 Wu, Q. 327 Tanaka, Y. 45 Terbojevich, M. 301 Yabuuchi, Y. 57 Tull, D. 195 Yadav, M.P. 93 Young, J.M. 275 Urbahns, K. 1 Usui, T. 57 Zagzoug, N.B. 323 Carbohydrate Research, 250 (1994) C11-—C13 Elsevier Science Publishers B.V., Amsterdam SUBJECT INDEX Acarviosin, synthesis and inhibitory activity of Chitosan samples, high-performance gel-per- eight analogues of methyl, containing a 1,6- meation chromatography of, 301 anhydro bridge, 177 Conformational features of cell-wall polysaccha- 2-Acetamido-1,4-imino-1,2,4-trideoxy-p-galacti- rides isolated from Alphanoascus mephitalus tol as competitive inhibitor of the human and related species, 289 lysosomal B-hexosaminidase A, 19 Conformationally biased isomaltosides as sub- Affinity labels for a B-glycosidase and a cellu- strate analogs for amyloglucosidase, 87 lase, N-bromoacetyl-glycopyranosylamines as, 195 1,3-Diamino-1,3-dideoxy-tetritols and their cyclic Affinity purification and characterisation of in- carbonic and thiocarbonic amides as compet- vertase from yeast using 2,5-dideoxy-2,5-im- itive inhibitors for glycoside hydrolases, 31 ino-p-mannitol and -p-glucitol as substrate Diazomethyl B-p-galactopyranosyl ketone, sui- analogs, 67 cide-substrate inactivation of B-galactosi- p-Aldopentoses, unprotected, Wittig reaction of dase, 101 with stabilized ylides: metal-ion effects, 231 2,5-Dideoxy-2,5-imino-p-mannitol and -p-gluci- p-Allose, p-altrose, p-gulose, and p-idose, NMR tol as glucosidase inhibitors, 67 studies of molybdate complexes of, 203 2,5-Dideoxy-2,5-imino-p-mannitol and p-glucitol Aminosubstituted a-p-glucosylmethylbenzenes from 5-azido-5-deoxy-p-glucofuranose and and an N-(C-a-p-glucosylmethyl)aniline, -L-idofuranose, a chemo-enzymic synthesis, novel a-p-glucosidase inhibitors, 161 67 Amylase from Streptomyces griseus, transglyco- Diels—Alder cycloaddition to unsaturated sug- sylation reaction of maltotriose-forming, 57 ars, stereocontrol in: reactivities of cis Amyloglucosidase substrate recognition as eval- dienophiles with cyclopentadiene, 261 uated from its interaction with conforma- Diels—Alder cycloaddition to unsaturated sug- tionally biased isomaltosides, 87 ars, stereocontrol in: reactivities of acyclic 1,2-Anhydro hexopyranoses, preparation from seven-carbon trans dienophiles derived from hexopyranose 2-tosylates by internal dis- aldopentoses, 249 placement, 327 N-Bromoacetyl-B8-p-glucopyranosylamine and Fucosylated and sialylated oligosaccharides hav- N-bromoacetyl-B-cellobiosylamine as affinity ing an N-acetyllactosaminyl core, chemoen- labels for a B-glucosidase and a cellulase, zymic synthesis, 129 195 Fucosyltransferase of human milk, use in the chemoenzymic synthesis of analogues of the sialyl Lewis* and sialyl Lewis* tetrasaccha- Cell-wall polysaccharides isolated from Apha- rides, 145 noascus mephitalus and related species, chemical structure and conformational features of, 289 (B-p-Galactopyranosylmethyl)amines, N-sub- Chemoenzymic synthesis of analogues of the stituted, as reversible inhibitors of B-p- sialyl Lewis* and sialyl* tetrasaccharides, 145 galactosidase, 93 Chemoenzymic synthesis of sialylated and fuco- B-p-Galactosidase, N-substituted (f-p-galac- svlated oligosaccharides having an N-acetyl- topyranosylmethyl)amines as reversible in- lactosaminyl core, 129 hibitors of, 93 C12 Subject index / Carbohydr. Res. 250 (1993) C11-—C13 B-Galactosidase, suicide-substrate inactivation B-Lactosides, a facile and regioselective synthe- of, by diazomethyl B-p-galactopyranosyl ke- sis of partially benzoylated 3,4-O-isopro- tone, 101 pylidene-, as standardized key intermediates B-Galactosidases of Escherichia coli with substi- for sialyl Lewis X (sLe*) analogues, cl tutions for GLU-461 can be activated, by Lipopolysaccharide, primary structure of the nucleophiles and can form #-p-galactosyl polysaccharide chain of virulent Pseu- adducts, 9 domonas solanacearum biotype I, 335 Galactosyl adducts, B-galactosidases of Es- Lipopolysaccharides of Pseudomonas solana- cherichia coli with substitutions for GLU-461 cearum, studies of O-specific polysaccharide can be activated by nucleophiles and can chains consisting of structurally different re- form B-p-, 9 peating units, 275 Gel-permeation chromatography of chitosan samples, high-performance, 301 Maltotriose-forming amylase from Streptomyces p-Glucopyranoside, synthesis of 2,3-di-O-glyco- griseus, transglycosylation reaction of, 57 syl derivatives of methyl a- and B-, 211 Metal-ion effects: Wittig reaction of unpro- B-Glucosidase and cellulase affinity labels, 195 tected p-aldopentoses with stabilized ylides, a-p-Glucosidase inhibitors, aminosubstituted 231 a-b-glucosylmethylbenzenes and an N-(C-a- Methyl acarviosin, synthesis and inhibitory activ- p-glucosylmethyl)aniline as novel, 161 ity of eight analogues containing a 1,6- C-(p-Glycopyranosyl)methylamines, synthesis anhydro bridge, 177 and inhibition studies of, 185 Methyl-5-(p-arabino-tetrahydroxybutyl)-3-furoyl- Glycosidase catalysis, hydrolysis of a- and B-p- hydrazine, reactions of 2-, 323 glucosyl fluoride by individual glucosidases: Methyl a- and B-p-glucopyranoside, synthesis new evidence for separately controlled of 2,3-di-O-glycosyl derivatives of, 211 “plastic” and “conserved” phases in, 45 Molybdate complexes of p-allose, p-altrose, p- Glycosidases, hydrolysis of glycosylpyridinium gulose, and p-idose, NMR studies of, 203 ions by anomeric-configuration-inverting, 79 Glycoside hydrolase inhibition by 1,3-diamino- 1,3-dideoxy-tetritols and their cyclic carbonic NMR studies of molybdate complexes of p-al- and thiocarbonic amides, 31 lose, p-altrose, p-gulose, and p-idose, 203 Glycosyl derivatives of methyl a- and B-p-gluco- Nojiritetrazoles, a new class of glycosidase in- pyranoside, synthesis of 2,3-di-O-, 211 hibitors, 113 Glycosylpyridinium ions, hydrolysis by anome- Nojiritetrazoles, selective transition state ana- ric-configuration-inverting glycosidases, 79 logue inhibitors of glycosidases, 113 Hexopyranose 2-tosylates and their facile con- (Phosphonomethy]!) analogue of 1d-myo-inositol version into 1,2-anhydro hexopyranoses by 3-(dihydrogenophosphate), synthesis of the internal displacement, 327 3-C-, 315 High-performance gel-permeation chromatogra- Plastic” and “conserved” phases in glycosidase phy of chitosan samples, 301 catalysis, hydrolysis of a-and B-p-glucosyl Hydrolysis of glycosylpyridinium ions by ano- fluoride by individual glucosidases: new evi- meric-configuration-inverting glycosidases, dence for separately controlled, 45 79 Polysaccharide chain of virulent Pseudomonas Hydrolysis of a- and B-p-giucosyl fluoride by solanacearum biotype II lipopolysaccharide, individual glucosidases: new evidence for primary structure, 335 separately controlled “plastic” and “con- Polysaccharide chains of Pseudomonas solanace- served” phases in glycosidase catalysis, 45 arum lipopolysaccharide consisting of struc- Inhibition studies and synthesis of C-(p-glyco- turally different repeating units, studies of pyranosyl)methylamines, 185 O-specific, 275 Inhibitors of a@-p-glucosidase, synthesis of Polysaccharides isolated from Aphanoascus aminosubstituted a-p-glucosylmethylben- mephitalus and related species, chemical zenes and an N-(C-a-p-glucosylmethyl)ani- structure and conformational features of line as, 161 cell-wall, 289 Inositol 3-(hydrogenphosphate), synthesis of the Pseudo-disaccharides as potential affinity re- 3-C-(phosphonomethy]) analogue of 1d-myo-, agents for trehalase, synthesis and evalua- 315 tion of diastereoisomeric alkylating, 1 Subject index / Carbohydr. Res. 250 (1993) C11-—C13 C13 Pseudomonas solanacearum biotype II lipopoly- Synthesis and inhibition studies of C-(p-glyco- saccharide, primary structure of the polysac- pyranosyl)methylamines, 185 charide chain of virulent, 335 Synthesis of 2-actamido-1,4-imino-1,2,4-tride- Pseudomonas solanacearum \ipopolysaccharides, oxy-b-galactitol and competitive inhibition of studies of O-specific polysaccharide chains the human lysosomal B-hexosaminidase A, consisting of structurally different repeating 19 units, 275 Synthesis of the 3-C-phosphonomethyl) analogue of ld-myo-inositol 3-(dihydrogeno- Reactions of 2-methyl-5-(p-arabino-tetrahydrox- phosphate), 315 ybutyl)-3-furoylhydrazine, 323 2-Tosylates of hexopyranoses, facile conversion Sialylated and fucosylated oligosaccharides hav- into 1,2-anhydro hexopyranoses by internal ing an N-acetyllactosaminyl core, chemoen- displacement, 327 zymic synthesis, 129 Transglycosylation reaction of maltotriose- Sialyl Lewis X (sLe*) analogues, a facile and forming amylase from Streptomyces griseus, regioselective synthesis of partially benzoy- 57 lated 3,4-O-isopropylidenated B-lactosides as Transition state analogue inhibitors of glycosi- standardized key intermediates for, cl dases, 113 Sialyl Lewis* and sialyl Lewis* tetrasaccharides, Trehalase, synthesis and evaluation of diastereo- use of human milk fucosyltransferase in the isomeric alkylating pseudo-disaccharides as chemoenzymic synthesis of analogues, 145 potential affinity reagents for, 1 Substitutions for GLU-461 can be activated by nucleophiles and can form B-p-galactosyl Unsaturated sugars, stereocontrol in Diels—Al- adducts, B-galactosidases of Escherichia coli der cycloaddition to: reactivities of acyclic with, 9 seven-carbon trans dienophiles derived from Sugar moiety of methyl acarviosin, synthesis and aldopentoses, 249 inhibitory activity of eight analogues contain- Unsaturated sugars, stereocontrol in Diels—Al- ing a 1,6-anhydro bridge obtained by chemi- der cycloaddition to: reactivities of cis cal modification of the, 177 dienophiles with cyclopentadiene, 261 Synthesis and evaluation of diastereoisomeric alkylating pseudo-disaccharides as potential Wittig reaction of unprotected p-aldopentoses affinity reagents for trehalase, 1 with stabilized ylides: metal-ion effects, 231