tritert-butylphosphanium

CC(C)n1cc(-c2ccc(C#N)cc2)c2ccc([N+](=O)[O-])cc21
Reaction #173357
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C1(NC(=O)c2ccc(OC)c(-c3c(F)cc(OC)c(Cl)c3F)c2)CCC(C)CC1
Reaction #184539
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN1CCN(c2ccc(N3CCC3)cc2C2CCC(C)(C)CC2)CC1
Reaction #186329
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(C=Cc2ccccc2)cc1
Reaction #189686
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1cc(-c2cc(NC(=O)OC(C)(C)C)c3ccnn3c2)cn1
Reaction #200132
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C1C2Cc3cc(OCc4c(F)ccc(-c5c(Cl)cccc5Cl)c4C)ccc3C21
Reaction #201938
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1onc(N)c1-c1cccnc1Oc1ccc(N)cc1
Reaction #213264
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccccc1-c1ccccn1
Reaction #230622
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NC(Cc1cccc(C#C[Si](C)(C)C)c1)C(CO)O[Si](C)(C)C(C)(C)C
Reaction #234516
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CC(C)(O)Cc1ccc(F)cc1
Reaction #242901
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C(C)=Cc1ccc(N(C)C)cc1
Reaction #251268
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(C)c(-c2cccc(C(F)(F)F)c2)c1
Reaction #252242
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #280840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C[Si](C)(C)C#Cc1ccc(C=O)cc1
Reaction #291732
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Clc1ncccc1-c1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
Reaction #294908
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)n1ccc2c(-c3cccnc3Oc3ccc(N)cc3)ccnc21
Reaction #314954
tert-butyl 4-(2-(4-aminophenoxy)pyridin-3-yl)-1-H-pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)(C)OC(=O)n1ccc2c(-c3cccnc3Oc3ccc(N)cc3)ccnc21
Reaction #314991
tert-Butyl 4-(2-(4-aminophenoxy)pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COC(=O)c1cc(OC)cc(C)c1N
Reaction #337101
methyl 2-amino-5-methoxy-3-methylbenzoate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COC(=O)C(C)(C)c1ccc2c(c1)N(S(=O)(=O)c1ccc(C(C)(C)C)cc1)Cc1ccc(C(F)(F)F)nc1N2
Reaction #368760
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(Oc2ncccc2-c2cnc(N)s2)cc1
Reaction #374108
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Seite 1Weiter