cyanide

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Reaction #10028
hydroxamic acids
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C1CCN(N2CCCCC2)CC1
Reaction #11324
piperidino-piperidine
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#CCc1csc2ccccc12
Reaction #80296
3-cyanomethylbenzothiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CN(C)CCc1c[nH]c2ccc(C#N)cc12
Reaction #158223
title product
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#CC(O)CCCCCCc1ccccc1
Reaction #173182
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CCC(=O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #173663
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cc(=O)n2nc(SCc3ccccc3)sc2n1
Reaction #174410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(C#N)CCC#CCOC1CCCCO1
Reaction #175200
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(N)c1ccc2c(c1)OCO2
Reaction #175789
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNC1(C#N)Cc2ccccc2C1
Reaction #175951
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC1OC(=O)c2cc(C#N)ccc21
Reaction #176092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc([N+](=O)[O-])cc1CC#N
Reaction #176267
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)ccc1C#N
Reaction #176688
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1cc2cnc(Nc3ccc(N4CCOCC4)cc3)nn2c1
Reaction #177616
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)cc1N
Reaction #178979
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(C(=O)NCC2(CC3CC3)CCC(S(=O)(=O)CC3CC3)CC2)c(C(F)(F)F)n1
Reaction #179201
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(N)(C#N)c1ccccc1
Reaction #179346
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC(O)CCCCCOc1cccc(F)c1
Reaction #179867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc2ccn3cccc3c(=O)c2c1
Reaction #180104
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCC(=C2c3cc(C#N)ccc3C=Cn3cccc32)CC1
Reaction #180543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي