21 件の反応に参加

918683

CN(C)c1ccc(N)c(SS(=O)(=O)O)c1
Reaction #44402
thiosulfuric acid S-{2-(amino)-5-(dimethylamino)-phenyl}ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)c1ccc(N)c(SS(=O)(=O)O)c1
Reaction #44403
thiosulfuric acid S-(2-amino-5-diethylamino-phenyl)ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2nc(S(C)(=O)=O)ccc2c1Br
Reaction #172962
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C=O)C1CCC2C(O)CCCC12C
Reaction #173090
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1nc(C)sc1I
Reaction #173845
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC(CC#C[Si](C)(C)C)C(C=O)O[Si](C)(C)C(C)(C)C
Reaction #174385
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOC(=O)Cc1ccc(-c2ccc(OCc3ccc(C(F)(F)F)c(OCC=C)c3C(=O)O)c(F)c2)cc1
Reaction #175405
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)C1=CC(O)(CCCCOc2ccccc2)C(=CC=CC(O)CCCO)C1=O
Reaction #176395
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCOCCOc1ccc(-c2ccc3c(c2)C=C(C(=O)Nc2ccc(S(=O)Cc4nnnn4C)cc2)CCN3CC(C)C)cc1
Reaction #177337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCOCCOc1ccc(-c2ccc3c(c2)C=C(C(=O)Nc2ccc(S(=O)Cc4nccn4CCO)cc2)CCN3CC(C)C)cc1
Reaction #177972
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(c1ccccc1)N1CC(CF)C(O)C1=O
Reaction #178161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1cc(I)cc2cnsc12
Reaction #178383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)COc1cc(C=CC=O)ccc1Cl
Reaction #178581
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CCc1cccc(CN2CCC3(CC2)CN(C(=O)c2cc4ccccc4s2)CCO3)c1F
Reaction #179883
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC1(CC2(c3cccc(Cl)c3)CO2)C(=O)c2ccccc2C1=O
Reaction #180347
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C1NC(=O)C2CSSCCC=CC(CC(=O)NC(Cc3cn(C(=O)OC(C)(C)C)c4ccccc34)C(=O)N2)OC(=O)CC1O
Reaction #180531
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N(CCc1ccccc1)Cc1ccc(CC=O)cc1
Reaction #180557
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(-n2ccnc(Sc3ccc(OC(F)(F)F)cc3)c2=O)ccc1OCC1(OP(=O)(OCc2ccccc2)OCc2ccccc2)CC(F)(F)C1
Reaction #180810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1[nH]ccnc1CN1CCC(S(=O)Cc2ccccc2F)CC1
Reaction #180990
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1csc(Cl)c1
Reaction #181536
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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