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COc1ccc2c(c1)[C@H]1Cc3ccccc3[C@H]1N2
Reaction #527020
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c2c(c1)[C@H]1Cc3ccccc3[C@H]1N2
Reaction #527030
title compound
Ausbeute 38.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)cc2c(c1C)[C@H]1Cc3ccccc3[C@H]1N2
Reaction #527031
title compound
Ausbeute 917.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)[C@H]1Cc3c(cc(C)c(OC)c3C)[C@H]1N2
Reaction #527037
cis-4b,5,9b,10-Tetrahydro-2,8-dimethoxy-1,3-dimethylindeno[1,2-b]indole
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c(C)c2c(c1C)[C@H]1Cc3ccccc3[C@H]1N2
Reaction #527057
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c2c(c1)[C@H]1Cc3cccc(C)c3[C@H]1N2
Reaction #527059
product
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc2c1Cc1c-2[nH]c2ccc(OC(F)(F)F)cc12
Reaction #1682651
title compound
Ausbeute 8.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2c(c1)C(=O)c1c-2[nH]c2ccc(OCc3ccccc3)cc12
Reaction #1847938
8-benzyloxy-2,4-dimethoxy-indeno[1,2-b]indol-10(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c2c(c1)C(=O)c1c-2[nH]c2ccc(OCc3ccccc3)cc12
Reaction #1847939
expected product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc2c1Cc1c-2[nH]c2ccc(OC(F)(F)F)cc12
Reaction #2024016
title compound
Ausbeute 8.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc2c3c([nH]c12)-c1ccccc1C3
Reaction #2168861
title compound
DOI: 10.6084/m9.figshare.5104873.v1