Recherche de Sous-structure

1086044

COCCOc1ccc2[nH]c3c(c2c1)CC1(C)C(=O)N(CCN(C)C)C(=O)N1C3c1cccc(O)c1
Reaction #69301
(3aSR,10RS)-2-(2-Dimethylamino-ethyl)-10-(3-hydroxy-phenyl)-6-(2-methoxy-ethoxy)-3a-methyl-3a,4,9,10-tetrahydro-2,9,10a-triaza-cyclopenta[b]fluorene-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc2[nH]c3c(c2c1)CC1(C)C(=O)N(CCBr)C(=O)N1C3c1cccc(O)c1
Reaction #69304
title compound
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)CC1(C)C(=O)N(CCBr)C(=O)N1C3c1cccc(O)c1
Reaction #69306
title compound
Rendement 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12Cc3c([nH]c4ccc(Cl)cc34)C(c3cccc(O)c3)N1C(=O)N(CCBr)C2=O
Reaction #69307
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12Cc3c([nH]c4ccc(OC(F)F)cc34)C(c3cccc(O)c3)N1C(=O)N(CCBr)C2=O
Reaction #69313
title compound
Rendement 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)CC1(C)C(=O)N(CCCCl)C(=O)N1C3c1cccc(O)c1
Reaction #69323
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3c(c2c1)C[C@@]1(C)C(=O)N(CCCCl)C(=O)N1[C@@H]3c1cccc(O)c1
Reaction #69324
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC12Cc3c([nH]c4ccc(OC(F)F)cc34)C(c3cccc(O)c3)N1C(=O)N(CCCCl)C2=O
Reaction #69325
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC12Cc3c([nH]c4ccc(Cl)cc34)C(c3cccc(O)c3)N1C(=O)N(CCCCl)C2=O
Reaction #69326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC12Cc3c([nH]c4ccc(Br)cc34)C(c3cccc(O)c3)N1C(=O)N(CCCCl)C2=O
Reaction #69327
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)Cc2c([nH]c3ccc(OC)cc23)C(c2cccc(O)c2)N1
Reaction #69329
(1RS,3RS)-1-(3-hydroxy-phenyl)-6-methoxy-3-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid methyl ester
Rendement 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc2[nH]c3c(c2c1)CC(C)(C(=O)OC)NC3c1cccc(O)c1
Reaction #69330
(1RS,3SR)-1-(3-hydroxy-phenyl)-6-ethoxy-3-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid methyl ester
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc2[nH]c3c(c2c1)CC(C)(C(=O)OC)NC3c1cccc(O)c1
Reaction #69331
(1RS,3RS)-1-(3-hydroxy-phenyl)-6-(2-methoxyethoxy)-3-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid methyl ester
Rendement 14.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(N)Cc1c[nH]c2ccc(OC)cc12
Reaction #69332
title compound
Rendement 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc2[nH]cc(CC(C)(N)C(=O)OC)c2c1
Reaction #69333
(+/−)-2-amino-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-propionic acid methyl ester
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc2[nH]cc(CC(C)(N)C(=O)OC)c2c1
Reaction #69334
(+/−)-2-amino-3-[5-(2-methoxy-ethoxy)-1H-indol-3-yl]-2-methyl-propionic acid methyl ester
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(Cc1c[nH]c2ccc(OC)cc12)[N+](=O)[O-]
Reaction #69335
title compound
Rendement 38.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc2[nH]cc(CC(C)(C(=O)OC)[N+](=O)[O-])c2c1
Reaction #69336
(+/−)-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-2-nitro-propionic acid methyl ester
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@](C)(Cc1c[nH]c2ccccc12)NC(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83116
title compound
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@](Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)O
Reaction #83117
acid
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
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