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C(Cl)(Cl)Cl

COc1ccc(CCN=C=O)cc1
Reaction #2933
4-methoxy-β-phenylethyl isocyanate
Ausbeute 0.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cccc(Cl)c2c(=O)o1
Reaction #3197
title compound
Ausbeute 250.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2[nH]c(=O)oc(=O)c12
Reaction #3209
title compound
Ausbeute 283.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(C(F)(F)F)cc(Cl)c2c(=O)o1
Reaction #3226
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ncc(C23CCCN2CCC3)cc1Cl
Reaction #3423
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(C)c2[nH]c(=O)[nH]c12
Reaction #5331
title compound
Ausbeute 4777.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6395
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC(C)C)C3)C(C)CCC1=O)C(C)CC2OC
Reaction #6396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10029
pure compound
Ausbeute 70.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10030
pure compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10031
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(C)c1ccccc1
Reaction #10033
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10035
product
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)N4CCCCC4)c3C2=O)C(=O)N1
Reaction #10153
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4- yl]methyl}piperidylcarboxamide
Ausbeute 145.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nn1c(=O)c2cc(F)c(F)c(Cl)c2n(C2CC2)c1=O
Reaction #10407
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(F)c(F)cc2c(=O)n1N(Cc1ccccc1)Cc1ccccc1
Reaction #10409
title compound
Ausbeute 198.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCc1ccncc1)C(=O)N(C)CCC12CC3CC(CC(C3)C1)C2
Reaction #11568
titled compound
Ausbeute 141.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)n1ncc(C(=O)O)c1Cl
Reaction #41134
1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)N2CCC(CS(C)(=O)=O)CC2)c1
Reaction #42587
title compound
Ausbeute 7.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(N5C[C@H]6CCCN6C5=O)c4)CC3)cccc2n1
Reaction #44175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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