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21923

FC(F)(F)Oc1ccc(-c2cccc3ccn(Cc4ccccc4)c23)cc1
Reaction #196453
DOI: 10.1039/C8SC04228D
Brc1cccc2ccn(Cc3ccccc3)c12
Reaction #240545
DOI: 10.1039/C8SC04228D
Fc1ccc(-c2cccc3ccn(Cc4ccccc4)c23)cc1Cl
Reaction #267204
DOI: 10.1039/C8SC04228D
FC(F)(F)Oc1ccc(-c2cccc3ccn(Cc4ccccc4)c23)cc1
Reaction #285272
DOI: 10.1039/C8SC04228D
Fc1cc(Br)c2c(ccn2Cc2ccc(C(F)(F)F)cc2)c1
Reaction #300516
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(CCCOc2cccc3ccccc23)c2cccc(Br)c2n1Cc1ccc(OC)cc1
Reaction #663474
ethyl 7-bromo-1-(4-methoxybenzyl)-3-(3-(naphthalen-1-yloxy)propyl)-1H-indole-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2c(C#N)c(CCCOc3cccc4ccccc34)c3cccc(Br)c32)cc1
Reaction #663475
7-bromo-1-(4-methoxybenzyl)-3-(3-(naphthalen-1-yloxy)propyl)-1H-indole-2-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2c(C#N)c(CCCOc3cccc4ccccc34)c3cccc(-c4ccccc4C)c32)cc1
Reaction #663476
1-(4-methoxybenzyl)-3-(3-(naphthalen-1-yloxy)propyl)-7-o-tolyl-1H-indole-2-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #954446
Ausbeute 0.0%DOI: 10.1039/C5SC04751J
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #954464
Ausbeute 0.0%DOI: 10.1039/C5SC04751J
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #954482
Ausbeute 0.0%DOI: 10.1039/C5SC04751J
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #954500
Ausbeute 0.0%DOI: 10.1039/C5SC04751J
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #954518
Ausbeute 0.0%DOI: 10.1039/C5SC04751J
O=C(O)CC1CCc2c1n(Cc1ccc(Cl)cc1)c1c(Br)cc(F)cc21
Reaction #1523394
title compound
Ausbeute 78.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCc2c1[nH]c1c(Br)cc(F)cc21
Reaction #1523395
(+/−)-(5-bromo-7-fluoro-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cc(F)cc2c3c(n(Cc4ccc(Cl)cc4)c12)C(CC(=O)O)CCC3
Reaction #1523397
desired acid
Ausbeute 61.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CC(=O)c2c1n(Cc1ccc(Cl)cc1)c1c(Br)cc(F)cc21
Reaction #1523398
ketone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCc2c(c3cccc(Br)c3n2C(=O)c2ccccc2)C1
Reaction #1692281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #1739253
Ausbeute 0.0%DOI: 10.1021/acs.accounts.0c00760
O=C(O)C[C@H]1CCc2c1n(Cc1ccc(Cl)cc1)c1c(N3CCCCC3)cc(F)cc21
Reaction #1739254
Ausbeute 0.0%DOI: 10.1021/acs.accounts.0c00760
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