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543100

C=CCOCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N1C(=O)c2ccccc2C1=O
Reaction #351104
compound 232
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccn(C[C@H](C)N3C(=O)c4ccccc4C3=O)n2)ccc1C#N
Reaction #959644
title compound
Ausbeute 25.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CBr)N1C(=O)c2ccccc2C1=O
Reaction #959648
title compound
Ausbeute 142.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccn(C[C@@H](C)N3C(=O)c4ccccc4C3=O)n2)ccc1C#N
Reaction #959649
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Cn1ccc(-c2ccc(C#N)c(C(F)(F)F)c2)n1)N1C(=O)c2ccccc2C1=O
Reaction #959736
title compound
Ausbeute 11.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1[C@H]1CCC[C@@H](O)C1
Reaction #1356969
cis-2-(3-hydroxycyclohexyl)-1H-isoindole-1,3(2H)-dione
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1[C@@H]1CCCC[C@H](O)[C@H]1Br
Reaction #2367891
title compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1[C@@H]1CCCC[C@H](O)C1
Reaction #2367892
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1CCCC(O)C1Br
Reaction #2367905
2-(2-bromo-3-hydroxy-cyclohexyl)-isoindole-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1CCCC(O)C1
Reaction #2367906
2-(3-hydroxy-cyclohexyl)-isoindole-1,3-dione
Ausbeute 79.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC[C@H](N2C(=O)c3ccccc3C2=O)[C@H](O)[C@H]1Br
Reaction #2367952
2-((1S,2S,3S)-3-bromo-2-hydroxy-4,4-dimethylcyclohexyl)isoindoline-1,3-dione
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC[C@H](N2C(=O)c3ccccc3C2=O)C[C@@H]1O
Reaction #2367953
2-((1S,3S)-3-hydroxy-4,4-dimethylcyclohexyl)isoindoline-1,3-dione
Ausbeute 20.4%DOI: 10.6084/m9.figshare.5104873.v1