AAAAAA

   
Results: 1-9 |
Results: 9
The search for anticancer agents at IDR
Authors: Kuszmann, J
Citation: J. Kuszmann, The search for anticancer agents at IDR, PHARMAZIE, 56, 2001, pp. S42-S49
Orally active antithrombotic thioglycosides, Part XIII - Conversion of 2,6-anhydro-D-altrose and -mannose derivatives with 4-substituted phenyl thiols to prepare compounds with potential antithrombotic activity
Authors: Bozo, E Boros, S Kuszmann, J
Citation: E. Bozo et al., Orally active antithrombotic thioglycosides, Part XIII - Conversion of 2,6-anhydro-D-altrose and -mannose derivatives with 4-substituted phenyl thiols to prepare compounds with potential antithrombotic activity, CARBOHY RES, 332(3), 2001, pp. 325-333
Synthesis of 4-substituted phenyl 3,6-anhydro-1,3-dithio-D-glucofuranosideand -pyranosides as well as 2,6-anhydro-1,2-dithio-alpha-D-altrofuranosides possessing antithrombotic activity
Authors: Bozo, E Boros, S Kuszmann, J
Citation: E. Bozo et al., Synthesis of 4-substituted phenyl 3,6-anhydro-1,3-dithio-D-glucofuranosideand -pyranosides as well as 2,6-anhydro-1,2-dithio-alpha-D-altrofuranosides possessing antithrombotic activity, CARBOHY RES, 329(3), 2000, pp. 525-538
Orally active antithrombotic thioglycosides, part XI. Synthesis of 4-cyano- and 4-nitrophenyl 2,5-anhydro-1,6-dithio-alpha-D-gluco- and -alpha-L-guloseptanosides carrying different substituents at C-3 and C-4
Authors: Bozo, E Boros, S Parkanyi, L Kuszmann, J
Citation: E. Bozo et al., Orally active antithrombotic thioglycosides, part XI. Synthesis of 4-cyano- and 4-nitrophenyl 2,5-anhydro-1,6-dithio-alpha-D-gluco- and -alpha-L-guloseptanosides carrying different substituents at C-3 and C-4, CARBOHY RES, 329(2), 2000, pp. 269-286
Synthesis of 4-substituted phenyl 2,5-anhydro-1,6-dithio-alpha-D-gluco- and -alpha-L-guloseptanosides possessing antithrombotic activity
Authors: Bozo, E Medgyes, A Boros, S Kuszmann, J
Citation: E. Bozo et al., Synthesis of 4-substituted phenyl 2,5-anhydro-1,6-dithio-alpha-D-gluco- and -alpha-L-guloseptanosides possessing antithrombotic activity, CARBOHY RES, 329(1), 2000, pp. 25-40
Synthesis of 4-cyanophenyl and 4-nitrophenyl 2-azido-2-deoxy-1,5-dithio-beta-D-arabino- and -beta-D-lyxopyranosides possessing antithrombotic activity
Authors: Bozo, E Kuszmann, J
Citation: E. Bozo et J. Kuszmann, Synthesis of 4-cyanophenyl and 4-nitrophenyl 2-azido-2-deoxy-1,5-dithio-beta-D-arabino- and -beta-D-lyxopyranosides possessing antithrombotic activity, CARBOHY RES, 325(2), 2000, pp. 143-149
Synthesis of 4-cyanophenyl and 4-nitrophenyl 2,6-anhydro-1,2-dithio-D-manno- and altropyranosides and their derivatives possessing antithrombotic activity
Authors: Bozo, E Boros, S Kuszmann, J
Citation: E. Bozo et al., Synthesis of 4-cyanophenyl and 4-nitrophenyl 2,6-anhydro-1,2-dithio-D-manno- and altropyranosides and their derivatives possessing antithrombotic activity, POL J CHEM, 73(6), 1999, pp. 989-1001
The fate of the methanesulfonyloxy group on reduction with LAH
Authors: Bozo, V Boros, S Kuszmann, J Gacs-Baitz, E
Citation: V. Bozo et al., The fate of the methanesulfonyloxy group on reduction with LAH, TETRAHEDRON, 55(26), 1999, pp. 8095-8102
Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-D-ribopyranosides as well as their 2-deoxy and 2,3-dideoxy derivatives possessing antithrombotic activity
Authors: Bozo, E Boros, S Kuszmann, J
Citation: E. Bozo et al., Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-D-ribopyranosides as well as their 2-deoxy and 2,3-dideoxy derivatives possessing antithrombotic activity, CARBOHY RES, 321(1-2), 1999, pp. 52-66
Risultati: 1-9 |