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81279

CCN1CC[C@]2(c3cccc(OC)c3)CC(=NO)CC[C@H]2C1
Reaction #2955
title compound
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1)C12OC1C1CCC2CC1
Reaction #8173
compound 11E
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
NN(C(=O)C12OC1C1CCC2CC1)c1ccc([N+](=O)[O-])c(C(F)(F)F)c1
Reaction #8174
compound 11F
Ausbeute 15.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(C(=O)NCCc2ccccc2C#N)C1
Reaction #46769
solid
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@]23CCCC[C@@H]2CN(CCCCc2ccccc2)CC3)c1
Reaction #54752
opaque oil
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@]23CCCC[C@@H]2C(=O)N(CC=C(C)C)C(=O)C3)c1
Reaction #54756
N-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)[C@@]1(c2ccccc2)C[C@@H]2C[C@H]1CC2O
Reaction #73469
desired product 89
DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)[C@@]1(c2ccccc2)C[C@@H]2C[C@H]1CC2Oc1cc2ccnc(OC)c2cc1Cl
Reaction #73470
desired product 90
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75284
12.4
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cn([C@H]3CC[C@H](N4CCNCC4C)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79850
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Br)ccc1Oc1ccccc1
Reaction #79853
4-Bromo-2-chloro-1-phenoxybenzene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(Cl)c2)OC1(C)C
Reaction #79854
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(Oc5ccccc5)c(Cl)c4)c4c(N)ncnc43)CC2)CC1
Reaction #79855
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1Oc1ccccc1
Reaction #79856
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(F)c2)OC1(C)C
Reaction #79857
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(Oc5ccccc5)c(F)c4)c4c(Cl)ncnc43)CC2)CC1
Reaction #79858
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1Oc1ccccc1
Reaction #79859
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn([C@H]3CC[C@H](N4CCN(C)CC4)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79861
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn([C@H]3CC[C@H](N4CCN(C)CC4)CC3)c3ncnc(N)c23)ccc1Oc1ccccc1
Reaction #79862
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Br)ccc1Oc1ccccc1
Reaction #79863
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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