bis(trimethylsilyl)azanide

COc1ccc(C(=O)CC(=O)c2c(F)cc(F)cc2F)cc1
Reaction #172967
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCn1cc(C(=O)C2CSC(c3cccnc3)N2C(=O)OC(C)(C)C)c2ccccc21
Reaction #173136
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C(c2c[nH]c3ccccc23)=C(c2cn3c4c(cccc24)CCC3)C(=O)N1c1ccccc1
Reaction #173185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1Nc2ccccc2C1=C1OCc2cc(Br)ccc21
Reaction #173237
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)[Si](C)(C)OCCCN(C1(C(=O)OCc2ccccc2)CCCC1)S(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #173345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C(=O)N1CC2CC(C)(C#N)CC2C1
Reaction #173396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOC(=O)C1(C)CCN(C(=O)C=Cc2ccc(OCC=C)c(OC)c2)CC1
Reaction #173674
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)Cc1cccc(C#N)c1
Reaction #173681
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(Br)cc2c1OCOCC2
Reaction #174571
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC1OC(=O)C1(CCCC)C(=O)OCc1ccccc1
Reaction #174655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)n1c(C(F)(F)F)cc2cccnc21
Reaction #174795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)c1cccc([N+](=O)[O-])c1
Reaction #175337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)NC(C1CC1)C(F)(F)S(=O)(=O)c1ccccc1
Reaction #175452
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)[Si](C)(C)OCCCCC1(C#N)CCN(C(=O)OCc2ccccc2)CC1
Reaction #175570
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(C2(C#N)CCC2)cc1
Reaction #175732
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C=CCCN1Cc1ccc(F)c(Cl)c1
Reaction #176847
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Cc1ccc(F)cc1)c1ccc(F)cc1
Reaction #177097
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(CCC)(Oc1ccc(Cl)cc1C1OCCO1)C(=O)OCC
Reaction #177486
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C=C(Cn1cccn1)c1cccc(C#N)c1
Reaction #177833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc2c(Nc3c(Cl)cc(C#CCNC(=O)N4CCOCC4)c4c3OCO4)ncnc2cc1OCCCN1CCOCC1
Reaction #177869
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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