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O=C(Cl)Oc1ccccc1

C#CCNC(=O)Nc1cc(NC(C)=O)c(F)cc1Cl
Reaction #1576
title product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3430
oil
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3cc(Br)ccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4137
product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCCc3ccccc32)CC1
Reaction #4141
product
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3ccccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4143
product
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3cc(Br)ccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4195
product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCCc3ccccc32)CC1
Reaction #4199
product
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCCc3ccccc32)CC1.O=C(O)/C=C\C(=O)O
Reaction #4201
product
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCSc1ccc(F)cc1)C(=O)Oc1ccccc1
Reaction #4292
N-[2-[(4-Fluorophenyl)thio]ethyl]-N-(1-methylethyl)carbamic acid phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN1CC=CCC1)Oc1ccccc1
Reaction #4455
N-(phenoxy- carbonylamino)-1,2,3,6-tetrahydropyridine
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCSc1cccc2nccn12)Oc1ccccc1
Reaction #5527
desired product
Ausbeute 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1OC(=O)Cl
Reaction #6999
2-methoxyphenyl chloroformate
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc([N+](=O)[O-])cc1)OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
Reaction #7758
desired product
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9388
solid
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1NC(=O)Oc1ccc([N+](=O)[O-])cc1
Reaction #11724
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc2cnccc12)Oc1ccccc1
Reaction #40685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc2ccc(O)cc12)Oc1ccccc1
Reaction #40686
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(NC(=O)Oc5ccccc5)c4)CC3)cccc2n1.Cl.Cl
Reaction #44089
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCOCC3)CC2)c2ccccc21
Reaction #44864
titled compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(C(=O)O)CCCC3)CC2)c2ccccc21
Reaction #44871
titled compound
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
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