Recherche de Sous-structure

7183

COC(=O)c1cc2ccc(O)cc2o1
Reaction #1151
methyl 6-hydroxybenzofuran-2-carboxylate
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@@]2(C)c3cc(Br)c(O)cc3N(C)[C@@H]12
Reaction #1864
cis-(±)-5-Bromo-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indol-6-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(O)c2)cc1
Reaction #2612
title compound
Rendement 76.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C=O)cc(O)c1O
Reaction #2664
expected product
Rendement 72.4%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(O)c(O)c(Cl)c1
Reaction #2665
expected product
Rendement 77.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(O)c(O)c([N+](=O)[O-])c1
Reaction #2666
expected product
Rendement 55.4%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(O)c(O)c(I)c1
Reaction #2667
expected product
Rendement 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1[nH]c2c(c1C)C[C@@H]1CN(CC)CC[C@@]1(c1cccc(O)c1)C2
Reaction #2957
title compound
Rendement 20.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)n1cc(C)c2c1C[C@]1(c3cccc(O)c3)CCN(CC)C[C@H]1C2
Reaction #2958
(±)-trans-Dipropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)OCC(C)C)c(C)c3C[C@@H]2C1.Cl
Reaction #2959
(±)-trans-2-(i-Butoxycarbonyl)-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)c1[nH]c2c(c1C)C[C@@]1(c3cccc(O)c3)CCN(C)C[C@@H]1C2
Reaction #2962
title compound
Rendement 49.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)NCc2ccccc2)[nH]c2c1C[C@@H]1CN(C)CC[C@@]1(c1cccc(O)c1)C2.Cl
Reaction #2964
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)Nc4ccccc4)c(C)c3C[C@@H]2C1
Reaction #2966
title compound
Rendement 22.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)N(C(C)C)C(C)C)c(C)c3C[C@@H]2C1.Cl
Reaction #2968
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)N(C)C)c(C)c3C[C@@H]2C1.Cl
Reaction #2972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)N4CCCC4)c(C)c3C[C@@H]2C1
Reaction #2974
title compound
Rendement 23.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(O)cccc2n1Cc1ccccc1
Reaction #3434
4-hydroxy-2-methyl-1-(phenylmethyl)-1H-indole
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(O)cccc2n1Cc1ccccc1-c1ccccc1
Reaction #3439
1-([1,1'-biPhenyl]-2-ylmethyl)-4-hydroxy-2-methyl-1H-indole
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(O)cccc2n1Cc1cccc(-c2ccccc2)c1
Reaction #3442
1-([1,1'-biphenyl]-3-ylmethyl)-4-hydroxy-2-methyl-1H-indole
Rendement 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(O)cccc2n1Cc1ccc(-c2ccccc2)cc1
Reaction #3444
1-([1,1'-biphenyl]-4-ylmethyl)-4-hydroxy-2-methyl-1H-indole
Rendement 77.4%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant