70 件の反応に参加

1434697

COc1ccccc1-c1ccc2c(c1)C(CNc1ccccc1)=CC(C)(C)N2
Reaction #54041
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3F)ccc2N1
Reaction #54076
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3-c3ccccc3)ccc2N1
Reaction #54080
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CSc1ccccc1-c1ccc2c(c1)C(CSCCc1ccccc1)=CC(C)(C)N2
Reaction #54081
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(OC)c(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)c1
Reaction #54082
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)c1
Reaction #54084
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)cc1
Reaction #54086
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)cc1OC
Reaction #54088
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(F)cc1-c1ccc2c(c1)C(CSCCc1ccccc1)=CC(C)(C)N2
Reaction #54090
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)C=C(CSCCc2ccccc2)c2cc(-c3ccccc3C(F)(F)F)ccc2N1
Reaction #54092
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1ccc(C(C)C)cc1-c1ccc2c(c1)C(CSCCc1ccccc1)=CC(C)(C)N2
Reaction #54094
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCSSCCc1ccccc1
Reaction #94344
2-phenylethyl-ethyl-disulphide
収率 111.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
OCCSCCc1ccccc1
Reaction #175367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)CC1NC(=O)OC1CCSCCc1ccccc1
Reaction #193792
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
BrCCCCCCSCCc1ccccc1
Reaction #238427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#CCNC(=O)C1CCCCC1CS(=O)(=O)c1ccc(SCCc2ccccc2)cc1
Reaction #258538
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1nc(SCCc2ccccc2)nc2c1ncn2Cc1ccccc1
Reaction #273104
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1ccc(SCCc2ccccc2)cc1
Reaction #288564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(CCCCc1c[nH]cn1)CCc1ccccc1
Reaction #364351
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)C1(c2ccc(-c3ccc(-c4onc(C)c4CSCCc4ccccc4)cc3)cc2)CC1
Reaction #369278
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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