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Results: 1-9 |
Results: 9
LIPOSOME ANCHORED VASCULAR ENDOTHELIAL GROWTH-FACTOR APTAMERS
Authors: WILLIS MC COLLINS B ZHANG T GREEN LS SEBESTA DP BELL C KELLOGG E GILL SC MAGALLANEZ A KNAUER S BENDELE RA GILL PS JANJIC N
Citation: Mc. Willis et al., LIPOSOME ANCHORED VASCULAR ENDOTHELIAL GROWTH-FACTOR APTAMERS, Bioconjugate chemistry, 9(5), 1998, pp. 573-582
LIPOSOME-ANCHORED VASCULAR ENDOTHELIAL, GROWTH-FACTOR APTAMERS (VOL 9, PG 573, 1998)
Authors: WILLIS MC COLLINS BD ZHANG T GREEN LS SEBESTA DP BELL C KELLOGG E GILL SC MAGALLANEZ A KNAUER S BENDELE RA GILL PS JANJIC N
Citation: Mc. Willis et al., LIPOSOME-ANCHORED VASCULAR ENDOTHELIAL, GROWTH-FACTOR APTAMERS (VOL 9, PG 573, 1998), Bioconjugate chemistry, 9(5), 1998, pp. 633-633
POST-SELEX COMBINATORIAL OPTIMIZATION OF APTAMERS
Authors: EATON BE GOLD L HICKE BJ JANJIC N JUCKER FM SEBESTA DP TARASOW TM WILLIS MC ZICHI DA
Citation: Be. Eaton et al., POST-SELEX COMBINATORIAL OPTIMIZATION OF APTAMERS, Bioorganic & medicinal chemistry, 5(6), 1997, pp. 1087-1096
STEREOSELECTIVE SYNTHESIS OF 2-DEOXY-BETA-GLYCOSIDES FROM GLYCAL PRECURSORS .1. STEREOCHEMISTRY OF THE REACTIONS OF D-GLUCAL DERIVATIVES WITH PHENYLSULFENYL CHLORIDE AND PHENYLSELENENYL CHLORIDE
Authors: ROUSH WR SEBESTA DP BENNETT CE
Citation: Wr. Roush et al., STEREOSELECTIVE SYNTHESIS OF 2-DEOXY-BETA-GLYCOSIDES FROM GLYCAL PRECURSORS .1. STEREOCHEMISTRY OF THE REACTIONS OF D-GLUCAL DERIVATIVES WITH PHENYLSULFENYL CHLORIDE AND PHENYLSELENENYL CHLORIDE, Tetrahedron, 53(26), 1997, pp. 8825-8836
STEREOSELECTIVE SYNTHESIS OF 2-DEOXY-BETA-GLYCOSIDES FROM GLYCAL PRECURSORS .2. STEREOCHEMISTRY OF GLYCOSIDATION REACTIONS OF 2-THIOPHENYL-ALPHA-D-GLUCO-PYRANOSYL AND 2-SELENOPHENYL-ALPHA-D-GLUCO-PYRANOSYL DONORS
Authors: ROUSH WR SEBESTA DP JAMES RA
Citation: Wr. Roush et al., STEREOSELECTIVE SYNTHESIS OF 2-DEOXY-BETA-GLYCOSIDES FROM GLYCAL PRECURSORS .2. STEREOCHEMISTRY OF GLYCOSIDATION REACTIONS OF 2-THIOPHENYL-ALPHA-D-GLUCO-PYRANOSYL AND 2-SELENOPHENYL-ALPHA-D-GLUCO-PYRANOSYL DONORS, Tetrahedron, 53(26), 1997, pp. 8837-8852
NOVEL NUCLEOSIDES VIA INTRAMOLECULAR FUNCTIONALIZATION OF 2,2'-ANHYDROURIDINE DERIVATIVES
Authors: MCGEE DPC SEBESTA DP OROURKE SS MARTINEZ RL JUNG ME PIEKEN WA
Citation: Dpc. Mcgee et al., NOVEL NUCLEOSIDES VIA INTRAMOLECULAR FUNCTIONALIZATION OF 2,2'-ANHYDROURIDINE DERIVATIVES, Tetrahedron letters, 37(12), 1996, pp. 1995-1998
2'-DEOXY-2'-ALKOXYLAMINOURIDINES - NOVEL 2'-SUBSTITUTED URIDINES PREPARED BY INTRAMOLECULAR NUCLEOPHILIC RING-OPENING OF 2,2'-O-ANHYDROURIDINES
Authors: SEBESTA DP OROURKE SS MARTINEZ RL PIEKEN WA MCGEE DPC
Citation: Dp. Sebesta et al., 2'-DEOXY-2'-ALKOXYLAMINOURIDINES - NOVEL 2'-SUBSTITUTED URIDINES PREPARED BY INTRAMOLECULAR NUCLEOPHILIC RING-OPENING OF 2,2'-O-ANHYDROURIDINES, Tetrahedron, 52(46), 1996, pp. 14385-14402
FACILE PREPARATION OF PERFLUORO-TERT-BUTYL ETHERS BY THE MITSUNOBU REACTION
Authors: SEBESTA DP OROURKE SS PIEKEN WA
Citation: Dp. Sebesta et al., FACILE PREPARATION OF PERFLUORO-TERT-BUTYL ETHERS BY THE MITSUNOBU REACTION, Journal of organic chemistry, 61(1), 1996, pp. 361-362
HIGHLY STEREOSELECTIVE SYNTHESIS OF ALPHA-L-OLIVOMYCOSIDES VIA TRIMETHYLSILYL TRIFLATE MEDIATED GLYCOSIDATIONS OF ,6-DIDEOXY-2-IODO-3-C-METHYL-ALPHA-L-MANNOPYRANOSE
Authors: ROUSH WR BRINER K SEBESTA DP
Citation: Wr. Roush et al., HIGHLY STEREOSELECTIVE SYNTHESIS OF ALPHA-L-OLIVOMYCOSIDES VIA TRIMETHYLSILYL TRIFLATE MEDIATED GLYCOSIDATIONS OF ,6-DIDEOXY-2-IODO-3-C-METHYL-ALPHA-L-MANNOPYRANOSE, Synlett, (4), 1993, pp. 264-266
Risultati: 1-9 |