Teilstruktursuche

C(C#N)C(=O)O

CCCC(C#N)(NC(C)=O)C(=O)OCC
Reaction #8715
Ethyl 2-acetylamino-2-cyanopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)CCCc1ccc(C(=O)OC)cc1
Reaction #50186
methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoate
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=C1CC(C)(C)NC(C)(C)C1
Reaction #54459
Ethyl 2,2,6,6-tetramethyl-4-piperidinylidene-cyanoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)C1CC(C)(C)NC(C)(C)C1
Reaction #54460
ethyl 2-(2,2,6,6-tetramethyl-4-piperidinyl)-cyanoacetate
DOI: 10.6084/m9.figshare.5104873.v1
C#CCNC(NCCSCc1[nH]cnc1C)=C(C#N)C(=O)OC
Reaction #55670
1-carbomethoxy-1-cyano-2-(2-propynylamino)-2-{2-[(4-methyl-1H-imidazol-5-yl)methylthio]ethylamino}ethylene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=CC1(C)CC1
Reaction #56720
ester
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)C(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73765
desired product
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73766
desired product
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnccc1CNS(=O)(=O)c1ccccc1S(=O)(=O)Oc1cc(C)cc(OCCCONC(=N)N)c1.Cl.Cl
Reaction #78006
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(CC(=O)O)CC(=O)O)c1
Reaction #78007
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)c2ccc(C(=O)O)cc2)c1
Reaction #78008
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(CCC(=O)O)Cc2ccccc2)c1
Reaction #78009
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C1CCN(Cc2ccccc2)C1)S(=O)(=O)c1ccccc1S(=O)(=O)Oc1cc(C)cc(OCCCONC(=N)N)c1.Cl.Cl
Reaction #78011
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)C2CCN(C)CC2)c1.Cl.Cl
Reaction #78012
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(C)Cc2cccnc2)c1.Cl.Cl
Reaction #78013
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCC#N)C1CCCCC1
Reaction #92784
4-Cyclohexylpentanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)(NC(C)=O)C1Cc2ccccc21
Reaction #161947
#99
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)Cc1ccc(Cl)c(F)c1
Reaction #169542
ethyl 3-(4-chloro-3-fluorophenyl)-2-cyanopropanoate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(c1ccccc1)C(C#N)C(=O)OC
Reaction #176960
DOI: 10.1039/C8SC04228D
CCCCC(CC)COC(=O)C(C#N)=C(c1ccccc1)c1ccccc1
Reaction #177892
DOI: 10.1039/C8SC04228D
Seite 1Weiter