Substructure Search

550836

C[C@@H](NC(=O)OC(C)(C)C)c1ccc(Nc2ncc3cc(-c4ccncc4)cc(Cl)c3n2)cc1
Reaction #207
Yield 51.0%
CC(C)(C)OC(=O)NC1(c2ccc(Br)cc2)CC1
Reaction #52481
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1(c2ccc(Br)cc2)CC1
Reaction #52482
1-(4-Bromophenyl)-cyclopropylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(OC2CN(c3ccc([C@H](C)N)cc3)C2)cc1
Reaction #68785
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)OC(C)(C)C)c1ccc(N2CC(Oc3ccc(OCC4CC4)cc3)C2)cc1
Reaction #68786
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)c1ccc(N2CC(Oc3ccc(OCC4CC4)cc3)C2)cc1
Reaction #68797
(S)-(1-{4-[3-(4-Cyclopropylmethoxy-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(c1ccc(Nc2nccc(-c3ccccc3)n2)cc1)C(F)(F)F
Reaction #69020
tert-butyl 2,2,2-trifluoro-1-(4-(4-phenylpyrimidin-2-ylamino)phenyl)ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(c2ccc(Br)cc2)CC1
Reaction #80046
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1(c2ccc(Br)cc2)CC1
Reaction #80047
1-(4-Bromophenyl)-cyclopropylamine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](C)NC(=O)OC(C)(C)C)cc1
Reaction #159573
title compound ( D2 )
Yield 176.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(c2ccc(Br)cc2)CC1
Reaction #159574
title compound ( D4 )
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C#Cc2ccc(C(C)NC(=O)OC(C)(C)C)cc2)cc1
Reaction #163352
{1-[4-(4-Ethoxy-phenylethynyl)-phenyl]ethyl}-carbamic acid tert-butylester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(C2=CCN(C(=O)OC(C)(C)C)CC2)cc1)N1CC[C@](CC(C)(C)O)(c2ccccc2)OC1=O
Reaction #168134
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H](C)N2CC[C@](CC(C)(C)O)(c3ccccc3)OC2=O)cc1
Reaction #168144
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(C(C)N3CCC(CC(C)(C)O)(c4ccccc4)OC3=O)cc2)nn1
Reaction #180129
DOI: 10.1039/C8SC04228D
C=CCC1(c2ccc(F)cc2)CCN(C(C)c2ccc(N3CCN(C)CC3)cc2)C(=O)O1
Reaction #182973
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccc(C(C)N3CCC(CC(C)(C)O)(c4ccccc4)OC3=O)cc2)ccn1
Reaction #183369
DOI: 10.1039/C8SC04228D
CC(c1ccc(Br)cc1)N1CCC(CC(C)(C)O)(c2ccccc2)OC1=O
Reaction #184863
DOI: 10.1039/C8SC04228D
CC(=O)CC1(c2ccccc2)CCN(C(C)c2ccc(Br)cc2)C(=O)O1
Reaction #185286
DOI: 10.1039/C8SC04228D
Cc1nc(-c2ccc(C(C)N3CCC(CC(C)(C)O)(c4ccccc4)OC3=O)cc2)sc1C
Reaction #185709
DOI: 10.1039/C8SC04228D
Page 1Next