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Results 1 to 25 of 838612

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PHENYLOXAZOLINE DERIVATIVES OF AMINO-SUGARS. II. THE FISSION OF PHENYLOXAZOLINES UNDER BASIC CONDITIONSGENT PA; GIGG R; SHAUNAGH MAY et al.1972; J. CHEM. SOC., PERKIN TRANS., 1; G.B.; DA. 1972; NO 21; PP. 2748-2750; BIBL. DISSEM.Serial Issue

BRANCHED-CHAIN SUGARS. XXVIII: SYNTHESIS OF 2-C-METHYL-L-GLYCERALDEHYDE, 2-C-METHYL-D-ERYTHROSE, AND 3-C-METHYL-L-ERYTHROSE DERIVATIVESYOSHIMURA J; HARA K; YAMAURA M et al.1982; BULL. CHEM. SOC. JPN.; ISSN 0009-2673; JPN; DA. 1982; VOL. 55; NO 3; PP. 933-937; BIBL. 13 REF.Article

SYNTHESIS OF 2-METHYL-(2-ACETAMIDO-4-O-ACETYL-6-O-BENZYL-3-O-(2-BUTENYL)-1,2-DIDEOX Y-ALPHA -D-GLUCOPYRANO)-(2,1-D)-2-OXAZOLINE, A VERSATILE INTERMEDIATE FOR THE SYNTHESIS OF COMPLEX OLIGOSACCHARIDES OF BACTERIAL CELLWALL, HUMAN MILK, AND BLOOD GROUP SUBSTANCESDURETTE PL; MEITZNER EP.1981; CARBOHYDR. RES.; ISSN 0008-6215; NLD; DA. 1981; VOL. 89; NO 2; PP. 279-288; BIBL. 25 REF.Article

SYNTHETIC STUDIES ON THE CARBOMYCINS (MAGNAMYCINS): AN EXCEPTION TO THE ENANTIOSELECTIVE SYNTHESIS OF BETA -ALKYL CARBOXYLIC ACIDS VIA CHIRAL OXAZOLINESZIEGLER FE; GILLIGAN PJ.1981; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1981; VOL. 46; NO 19; PP. 3874-3880; BIBL. 28 REF.Article

Highly selective synthesis of aldonolactones from protected alditols by ruthenium complex-catalyzed dehydrogenation. A method of converting aldopentoses to their stereoisomersSABURI, M; ISHII, Y; KAJI, N et al.Chemistry Letters. 1989, Num 4, pp 563-566, issn 0366-7022Article

Novel 1,6-anhydro-β-lactose derivatives for rapid and efficient syntheses of oligosaccharide sequences containing N-acetyllactosamineNISHIMURA, S; MURAYAMA, S; KURITA, K et al.Chemistry Letters. 1992, Num 8, pp 1413-1416, issn 0366-7022Article

Efficient syntheses of D-psico- and D-sorbo-furanosesFAIVRE-BUET, V; EYNARD, I; NTEDE NGA, H et al.Journal of carbohydrate chemistry. 1993, Vol 12, Num 3, pp 349-356, issn 0732-8303Article

Hydroxymethylation of aldonolactones and a chemical synthesis of 3-deoxy-3-fluoro-D-fructoseBOLS, M; GRUBBE, H; JESPERSEN, T. M et al.Carbohydrate research. 1994, Vol 253, pp 195-206, issn 0008-6215Article

Chirale Bausteine aus Kohlenhydraten. XI: 2-Lithio-1,3-dithian-induzierte Reaktionen an 5,6-Didesoxy-5-iodhexofuranosen zu offenkettigen Heptosetrimethylen-dithioacetalen = Eléments chiraux à partir d'oses. XI: Réactions de didésoxy-5,6 iodo-5 hexofuranoses induites par le lithio-2 dithianne-1,3 conduisant à des heptoses triméthylène dithioacétals à chaîne ouverte = Chiral building units from carbohydrates. XI: 2-Lithio-1,3-dithiane-induced reactions of 5,6-dideoxy-5-iodohexofuranoses leading to open-chained heptose trimethylene dithioacetalsREDLICH, H; LENFERS, J. B; BRUNS, W et al.Liebigs Annalen der Chemie. 1985, Num 8, pp 1570-1586, issn 0170-2041Article

Synthesis of C(6)-carboxylate analogues of N-acetylmuramic acidHECKER, S. J; MINICH, M. L.Journal of organic chemistry. 1990, Vol 55, Num 24, pp 6051-6054, issn 0022-3263, 4 p.Article

Acid-catalysed transformation of α-trifluoromethanesulfonates of γ- and δ-lactones into 2,5-disubstituted homochiral tetrahydrofuransWHEATLEY, J. R; BICHARD, C. J. F; MANTELL, S. J et al.Journal of the Chemical Society. Chemical communications. 1993, Num 13, pp 1065-1067, issn 0022-4936Article

BAUSTEINE VON OLIGOSACCHARIDEN. XXXI: SYNTHESE DER REPEATING-UNIT DER O-SPEZIFISCHEN KETTE DES LIPOPOLYSACCHARIDES DES BAKTERIUMS ESCHERICHIA COLI 075 = ELEMENTS DES OLIGOHOLOSIDES. XXXI: SYNTHESE DU MOTIF DE REPETITION DE LA CHAINE O-SPECIFIQUE DU LIPOPOLYOSIDE D'ESCHERICHIA COLI 075PAULSEN H; LOCKHOFF O.1981; CHEM. BER.; ISSN 0009-2940; DEU; DA. 1981; VOL. 114; NO 9; PP. 3115-3125; ABS. ENG; BIBL. 6 REF.Article

Formation of disacharides related to heparin and heparan sulfate by chemical modification of maltoseGLUSHKA, J. N; PERLIN, A. S.Carbohydrate research. 1990, Vol 205, pp 305-321, issn 0008-6215, 17 p.Article

SYNTHESIS OF SOME DISACCHARIDES CONTAINING PENT-2-ENOPYRANOSE RESIDUESGRYNKIEWICZ G.1980; CARBOHYD. RES.; NLD; DA. 1980; VOL. 80; NO 1; PP. 53-62; BIBL. 17 REF.Article

Synthesis of four spacer-containing trisaccharides with the 4-O-(β-L-rhamnopyranosyl)-D-glucopyranose unit in common, representing fragments of capsular polysaccharides from Streptococcus pneumoniae types 2, 7F, 22F, and 23FVAN STEIJN, A. M. P; VLIEGENTHART, J. F. G et al.Journal of carbohydrate chemistry. 1992, Vol 11, Num 6, pp 665-689, issn 0732-8303Article

A synthetic approach to squalestatin 1HESHAM ABDEL-RAHMAN; ADAMS, J. P; BOYES, A. L et al.Journal of the Chemical Society. Chemical communications. 1993, Num 24, pp 1839-1841, issn 0022-4936Article

SYNTHESIS OF NEW-BRANCHED-CHAIN CYCLITOLS HAVING EPI AND ALLO CONFIGURATION AND MYO CONFIGURATION RESPECTIVELY FROM 3-O-BENZYL-5,6-DIDEOXY-5-(C-(1,3-DITHIAN-2-YL))-6-NITRO-D-ALLOFURANOSE AND -L-TALOFURANOSEFLINABASHI M; KOBAYASHI K; YOSHIMURA J et al.1979; J. ORG. CHEM.; USA; DA. 1979; VOL. 44; NO 10; PP. 1618-1621; BIBL. 8 REF.Article

Convenient oxidative debenzylation using dimethyldioxiraneCSUK, R; DÖRR, P.Tetrahedron (Oxford. Print). 1994, Vol 50, Num 33, issn 0040-4020, viii, 9983-9988 [7 p.]Article

Fluorination at position 6 of derivatives of methyl α-D-galactopyranosideMULARD, L. A; KOVAC, P; GLAUDEMANS, C. P. J et al.Carbohydrate research. 1994, Vol 259, Num 1, pp 117-129, issn 0008-6215Article

Kronenether mit Triose- und Pentose-Bausteinen = Ethers crown avec les squelettes triose et pentose = Crown ethers with triose and pentose structural unitsALDAG, R; SCHRÖDER, G.Liebigs Annalen der Chemie. 1984, Num 5, pp 1036-1045, issn 0170-2041Article

Synthesis and biological activities of N-acetyl-1-thiomuramoyl-L-alanyl-D-isoglutamine and some of its lipophilic derivativesHASEGAWA, A; HIOKI, Y; KISO, M et al.Carbohydrate research. 1983, Vol 123, Num 2, pp 183-199, issn 0008-6215Article

Stereoselective access to α-azido aldehydes and a new synthetic route to myriocinDELOISY, S; TON THAT THANG; OLESKER, A et al.Bulletin de la Société chimique de France. 1996, Vol 133, Num 6, pp 581-585, issn 0037-8968Article

PARTIALLY BENZYLATED OXAZOLINE DERIVATIVES OF 2-ACETAMIDO-2-DEOXY-D-GLUCOPYRANOSE AS STANDARDIZED INTERMEDIATES FOR OLIGOSACCHARIDE SYNTHESIS. PREPARATION OF DISACCHARIDES HAVING THE SEQUENCES BETA -D-GLCPNAC(1->X)-D-GAL AND BETA -D-GLCPNAC(1->4)-D-GLCNACNASHED MA; KISO M; SLIFE CW et al.1981; CARBOHYDR. RES.; ISSN 0008-6215; NLD; DA. 1981; VOL. 90; NO 1; PP. 71-82; BIBL. 23 REF.Article

CHIRAL 1,4-DIHYDROPYRIDINES. SYNTHESIS AND ABSOLUTE CONFIGURATIONMEYERS AI; NATALE NR; WETTLAUFER DG et al.1981; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1981; VOL. 22; NO 51; PP. 5123-5126; BIBL. 11 REF.Article

SYNTHETIC ROUTES TO 3-C-CYANO-3-DEOXY-D-GALACTOPYRANOSE DERIVATIVESAZEEZ MUBARAK; FRASER REID B.1982; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1982; VOL. 47; NO 22; PP. 4265-4268; BIBL. 14 REF.Article

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