palladium(2+)

Cc1cc2c(cc1C#C[Si](C)(C)C)C(C)(C)CCS2
Reaction #6632
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COCCCOc1nc(-c2c(C)cccc2C)nc2c1CN(c1cc(C(C)C)ccc1C)CC2
Reaction #168000
2-(2,6-dimethylphenyl)-6-(5-isopropyl-2-methylphenyl)-4-(3-methoxypropoxy)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOCCn1nc(CC)c(N)c1C(N)=O
Reaction #173066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(Cc1ccc(O)cc1)Oc1ccccc1
Reaction #173127
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)C#Cc1ccc(C=O)cc1
Reaction #173144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(CC)c1cc(C)nn2c(-c3cc4cc(C)ccc4n3C)c(C)nc12
Reaction #173146
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccccc1)c1cn2cc(-c3ccoc3)ccc2n1
Reaction #173540
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCC1CNCC1c1ccccc1
Reaction #173586
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)n1ccc2c(NC(=O)C3CCNCC3)ccnc21
Reaction #173717
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccccc1Oc1ccnc2ccccc12
Reaction #173739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)N1C(=O)C=C(c2ccc(CC(C(=O)c3ccccc3)c3ccccc3)cc2Br)S1(=O)=O
Reaction #173887
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCN(c2cccc3cc(F)ccc23)CC1
Reaction #173940
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCN(CCC)c1ccnc(N=C(c2ccccc2)c2ccccc2)c1
Reaction #174090
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)C(=O)C=C(C)c1ccc(OC(C)c2ccccc2)c2oc(C(C)=O)cc12
Reaction #174116
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCc1cc(-c2ccc3c(cnn3C)c2)c(OC2Cc3ccccc3C2)cc1C#N
Reaction #174191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCc2cccc(Nc3cc(Nc4ccnn4C)ncc3Cl)c2C1=O
Reaction #174221
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCc1ccccc1
Reaction #174279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1c(N)nc(-c2ccc(Cl)c(OC)c2F)nc1C(=O)OC
Reaction #174382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CC(=O)NN=C1c1ccc(NC(=O)CCNCC(O)COc2ccc(CCOCC3CC3)cc2)cc1
Reaction #174428
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cn1c(CCc2ccc(F)cc2)c(C2CC2)c(=O)n1-c1ccc(F)cc1
Reaction #174430
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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