dicyclohexylamine

C=CC(=O)N(C1CCCCC1)C1CCCCC1
Reaction #5588
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C[Si](C)(C)C#Cc1ccc(C=O)cc1
Reaction #42158
4-[(trimethylsilyl)ethynyl]benzaldehyde
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)c1ccccc1C#CC(C)(C)O
Reaction #42159
4-(N,N-dimethylaminophenyl)-2-methyl-3-butyne-2-ol
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#CC(C)(O)Cc1ccc(F)cc1
Reaction #42160
(4-fluorophenyl)-2-methyl-3-butyne-2-ol
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[Si](C)(C)C#Cc1ccc(C=O)cc1
Reaction #42177
4-[(trimethylsilyl)ethynyl]benzaldehyde
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)c1ccccc1C#CC(C)(C)O
Reaction #42178
4-(N,N-dimethylaminophenyl)-2-methyl-3-butyne-2-ol
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#CC(C)(O)Cc1ccc(F)cc1
Reaction #42179
(4-fluorophenyl)-2-methyl-3-butyne-2-ol
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C1CCC([NH2+]C2CCCCC2)CC1.O=C([O-])c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-]
Reaction #55600
product
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(=O)S[C@@H](CC(C)C)C(=O)O
Reaction #74191
title compound
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C1CCC([NH2+]C2CCCCC2)CC1.O=C([O-])c1cc(Oc2ccc(C(F)(F)F)cc2Cl)ccc1[N+](=O)[O-]
Reaction #93612
product
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
NC(=O)c1nc(F)cnc1O
Reaction #173614
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)Oc1cc(N2C(=O)C3=C(CCCC3)C2=O)c(F)cc1Cl
Reaction #179327
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1nccs1)N(C1CCCCC1)C1CCCCC1
Reaction #186149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CC(C)(O)Cc1ccc(F)cc1
Reaction #190338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(C)OCOc1cc2ccc(-c3ccc(C(=O)O)cc3)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #196937
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(SC(=O)c1ccccc1)C(=O)N(CC(=O)O)C1CC1
Reaction #214811
N-(2-Benzoylthiopropanoyl)-N-cyclopropylglycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCOP(=O)(CC(=O)C1CCCN(C(=O)OCc2ccccc2)C1C(=O)OCc1ccccc1)OCC
Reaction #217100
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
C=C1CCCC(C(=O)OCC[Si](C)(C)C)(c2cccc(C(C)(C)C)c2)C1
Reaction #219282
1-(3-tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Cc1csc(C(O)=S)n1
Reaction #223134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C1CCC(NC2CCCCC2)CC1
Reaction #231292
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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