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1337

N#CCC1CCN(Cc2ccccc2)C1
Reaction #962
product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1oc(-c2ccccc2)nc1COc1ccc2oc(CCCC#N)cc2c1
Reaction #1149
2-(3-cyanopropyl)-5-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)c(F)cc(F)c1C#N
Reaction #1368
2-methyl-3,4,6-trifluorobenzonitrile
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(O)c1ccc(Cl)c(Cl)c1
Reaction #1933
expected product
Ausbeute 100.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ncc(C#N)cn2)cc1
Reaction #2392
4-tert-butyl-N-{6-[2-(5-cyanopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(CO)cs1
Reaction #2844
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cccc(CCCC#N)c2c1
Reaction #2984
4-(7-METHOXY-1-NAPHTHYL)BUTYRONITRILE
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)CCCCCC#N
Reaction #3431
expected product
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2cc(Br)cc(C#N)c21
Reaction #5024
compound
Ausbeute 81.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CC#N)cc1C
Reaction #5119
3,4-dimethylbenzyl cyanide
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H]1C[C@H](CC#N)OC(C)(C)O1
Reaction #5782
(±)-cis-2,2-dimethyl-6-(2-propenyl)-1,3-dioxane-4-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H]1C[C@H](CC#N)OCO1
Reaction #5798
(±)-cis-6-(2-propenyl)-1,3-dioxane-4-acetonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCC=C2C#N
Reaction #6483
title compound
Ausbeute 60.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC1=C(C#N)c2ccccc2CC1
Reaction #6496
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC1=C(C#N)c2cccc(OC)c2CC1
Reaction #6497
title compound
Ausbeute 70.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(CC#N)c2c1C
Reaction #6841
(5-methoxy-4-methyl-1H-indol-3-yl)-acetonitrile
Ausbeute 87.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2c(c1)CCC(=O)N2
Reaction #6909
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Oc2ccc(Cl)c(Cl)c2)c(C=O)c1
Reaction #6992
title product
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(C)c1nnc(-c2ccc(-c3ccccc3)nc2)n1-c1ccccc1C#N
Reaction #7027
compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(S(N)(=O)=O)s1
Reaction #7053
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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