Recherche de Similitude

425521

CC(C)(C)OC(=O)N1C(Cc2ccc(N)cc2)CCC1C(O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #284265
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(Cc2ccc(N)cc2)CCC1C(O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #298082
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(Cc2ccc(N)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #330832
title compound
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H](Cc2ccc(N)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #330833
Tert-butyl (2S,5R)-2-(4-aminobenzyl)-5-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(phenyl)methyl]pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H](Cc2ccc(N)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #330842
Tert-butyl (2S,5R)-2-(4-aminobenzyl)-5-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(phenyl)methyl]pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(Cc2ccc(N)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1cccc(Cl)c1
Reaction #330843
title compound
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(Cc2ccc(NC(=O)Cc3csc(N)n3)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #330915
product
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #330916
product
Rendement 21.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #330917
product
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)Nc1ccc(C[C@H]2CC[C@@H]([C@H](O[Si](C)(C)C(C)(C)C)c3cccc(F)c3)N2C(=O)OC(C)(C)C)cc1)c1cscn1
Reaction #330920
Tert-butyl (2S,5R)-2-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(3-fluorophenyl)methyl]-5-(4-{[2-(1,3-thiazol-4-yl)propanoyl]amino}benzyl)pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)c1ccc(CC2CCC(C(O[Si](C)(C)C(C)(C)C)c3ccccc3)N2C(=O)OC(C)(C)C)cc1)c1ccccn1
Reaction #379871
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(Cc2ccc(N)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #490621
title compound
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H](Cc2ccc(N)cc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #490622
Tert-butyl(2S,5R)-2-(4-aminobenzyl)-5-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(phenyl)methyl]pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #490633
solid
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H](Cc2ccc(N)c(N)c2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #490634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(Cc2ccc(N)cc2)CCC1C(O[Si](C)(C)C(C)(C)C)c1cccc(Cl)c1
Reaction #754141
DOI: 10.1039/C8SC04228D
CN(CCc1ccccn1)C(=O)c1ccc(CC2CCC(C(O[Si](C)(C)C(C)(C)C)c3ccccc3)N2C(=O)OC(C)(C)C)cc1
Reaction #754912
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1[C@H](Cc2ccc(N)nc2)CC[C@@H]1[C@H](O[Si](C)(C)C(C)(C)C)c1ccccc1
Reaction #800883
title compound
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@H](Cc2ccc(N)nc2)CC[C@@H]1[C@H](O)c1ccccc1
Reaction #800884
title compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C[C@@H]2CC[C@H]([C@H](O)c3ccccc3)N2C(=O)OC(C)(C)C)cn1
Reaction #800890
title compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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