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1012175

O=[N+]([O-])c1ccc(-c2ccccc2)cc1
Reaction #64999
desired product
Ausbeute 127.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccccc1-c1ccc2c(c1C=O)OCO2
Reaction #70965
5-(2-Formylphenyl)-1,3-benzodioxole-4-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([C@@H]2c3cc4c(cc3[C@@H](O[C@@H]3O[C@@H]5CO[C@@H](C)O[C@H]5[C@H](O)[C@H]3O)[C@H]3COC(=O)[C@H]23)OCO4)cc(OC)c1O
Reaction #92883
Etoposide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(-c2ncccc2[N+](=O)[O-])c(C)c1
Reaction #213005
DOI: 10.1039/C8SC04228D
O=C1C(Cc2c(Cl)cc(-c3cccnc3)cc2Cl)CCN1C1CCC(F)CC1
Reaction #241628
DOI: 10.1039/C8SC04228D
CC1=CC(C(C)(C)C)=CC1=C(c1ccc(C)cc1)c1ccc(C)cc1
Reaction #261318
DOI: 10.1039/C8SC04228D
COc1cccc2c(C3=C(c4cn(C)c5cc(-c6ccc(Cl)cc6)c(F)cc45)C(=O)NC3=O)coc12
Reaction #261586
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(O)cc1[N+](=O)[O-])OCCCCl
Reaction #274101
DOI: 10.1039/C8SC04228D
CCOC(=O)CCc1cc(F)cc(F)c1
Reaction #281202
DOI: 10.1039/C8SC04228D
O=C(Nc1cnccn1)Nc1ccccc1OC(F)F
Reaction #291377
DOI: 10.1039/C8SC04228D
C=CCCc1ccc(C2CCCCC2)cc1
Reaction #325065
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C)=CC1=C(c1ccc(C(C)(C)C)cc1)c1ccc(C(C)(C)C)cc1
Reaction #374025
DOI: 10.1039/C8SC04228D
COC(C)C(C)C(OC)OC
Reaction #379212
DOI: 10.1039/C8SC04228D
FC(F)(F)c1cccc(Oc2ccnc(C3CC3)n2)c1
Reaction #499013
pure product
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)Nc1ccc(Br)n(Cc2cncc(C(=O)c3ccc(F)cc3)c2)c1=O)N(C)C(=O)OCc1ccccc1
Reaction #643452
((S)-1-{6-bromo-1-[5-(4-fluoro-benzoyl)-pyridin-3-ylmethyl]-2-oxo-1,2-dihydro-pyridin-3-ylcarbamoyl}-ethyl)-methyl-carbamic acid benzyl ester
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(-n2cc([N+](=O)[O-])nc2C)c(C)c1
Reaction #671982
title compound
Ausbeute 70.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(-c2ncccc2[N+](=O)[O-])c(C)c1
Reaction #671988
title compound
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(C2([N+](=O)[O-])C=CC=CC2C)c(C)c1
Reaction #671995
title compound
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)n1ccc2c(C)nc3cc(-c4c(C)cc(C)cc4C)ccc3c21
Reaction #672022
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)C(=S)Nc1cc(Cl)cc(Cl)c1
Reaction #750034
DOI: 10.1039/C8SC04228D
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