2-methylpropan-2-olate

O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #40649
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=S)C(CC(C(=O)c1ccc(Cl)cc1Cl)c1ncc[nH]1)c1ccccc1
Reaction #60132
methyl 5-(2,4-dichlorophenyl)-4-imidazol-2-yl-5-oxo-2-phenylthiopentanoate
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=CC=Cc1cc(Br)cc(Br)c1
Reaction #71529
3-(3′,5′-dibromophenyl)-2-propenal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C=C(C)Oc1cccc(C)c1
Reaction #173016
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1nc(OC2CCCCC2)nc2c1ncn2C1CCCCO1
Reaction #173028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(Cn2nnc3ccccc32)cc1
Reaction #173134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CC2CN(c3cncc(Br)c3)CC2C1
Reaction #173143
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(NC(=O)c1cc(Cl)ccc1NC(=O)c1cc(Br)nn1-c1ncccc1Cl)C1CC1
Reaction #173199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(c1ccc(C(=O)OC)cc1)C(C(=O)OC(C)(C)C)c1ccc(Cl)cc1
Reaction #173270
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1nccc(N2CCn3c2cc(-c2ccccc2)cc3=O)n1
Reaction #173303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSC(=NC[Si](C)(C)C)c1ccc(COC(C)=O)c2ccccc12
Reaction #173435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc2c1C(=O)CCCN2C(=O)OC(C)C
Reaction #173456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCC1=C(C)C(O)CC1=C
Reaction #173706
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1nc(CC)n(-c2ccc(N3CCC4(CC3)OCCO4)cc2)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #173934
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)
COC(=O)c1ccc(N2CCCCCS2(=O)=O)c(C)c1
Reaction #173970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cnc(N=C(c2ccccc2)c2ccccc2)nc1NCc1cc2cccc(Cl)c2nc1-c1ccccc1Cl
Reaction #174053
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)
CCSc1cccc2nn(C)c(S(N)(=O)=O)c12
Reaction #174187
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(S(=O)(=O)n2cc(C(C)C)c3ccccc32)cc1
Reaction #174236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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