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5323

CC(C(=O)O)S(=O)(=O)NCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11737
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Sc1ncccc1-c1ccc(C#N)c2ccccc12
Reaction #74056
ethyl 2-(3-(4-cyanonaphthalen-1-yl)pyridin-2-ylthio)-2-methylpropanoate
収率 36.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Sc1ncccc1-c1ccc(C#N)c2ccccc12)C(=O)O
Reaction #74057
2-(3-(4-cyanonaphthalen-1-yl)pyridin-2-ylthio)-2-methylpropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(C(=O)O)S(C)(=O)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77814
aimed product
収率 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CCCCCCC(=O)O)S(C)(=O)=O
Reaction #93915
title compound
収率 110.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCCC(CC#CCCCC(=O)O)S(C)(=O)=O
Reaction #93921
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)O)S(=O)(=O)C1CCCCC1
Reaction #160412
2-cyclohexanesulfonyl-2-methyl-propionic acid
収率 95.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)ccn(CCC(C)(C(=O)O)S(C)(=O)=O)c1=O
Reaction #171459
2-methyl-4-(3-methyl-2-oxo-4-phenylpyridin-1(2H)-yl)-2-(methylsulfonyl)butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)ccn(CCC(C)(C(=O)NOC2CCCCO2)S(C)(=O)=O)c1=O
Reaction #171460
2-methyl-4-(3-methyl-2-oxo-4-phenylpyridin-1(2H)-yl)-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(N(CCc2cccc(F)c2)C(=O)Nc2ncc(SC(C)(C)C(=O)O)s2)CC1
Reaction #175315
DOI: 10.1039/C8SC04228D
CCCCOC(=O)c1cc(NC(=O)C2=C(C)OCCS2)ccc1Cl
Reaction #176806
DOI: 10.1039/C8SC04228D
CC1CCC(N(CCCc2cccc(C(F)(F)F)c2)C(=O)Nc2ncc(SCC(=O)O)s2)CC1
Reaction #189185
DOI: 10.1039/C8SC04228D
O=C(O)CSc1nc2cc(-c3ccc(-c4ccccc4O)cc3)c(Cl)cc2[nH]1
Reaction #189650
DOI: 10.1039/C8SC04228D
CC1CCC(N(CCCc2coc3ccc(Cl)cc23)C(=O)Nc2ncc(SCC(=O)O)s2)CC1
Reaction #190173
DOI: 10.1039/C8SC04228D
CCC(CCC(F)(F)C(F)(F)F)(C(=O)OC)S(=O)(=O)CCC(F)(F)F
Reaction #192071
DOI: 10.1039/C8SC04228D
CC(C)(Sc1nc(CCOc2ccc(C(=O)Nc3ccccc3)cc2)cs1)C(=O)O
Reaction #195689
DOI: 10.1039/C8SC04228D
O=C(CSc1ccc(C(=O)Nc2ccc(F)cc2)cn1)OCc1cccc(F)c1
Reaction #196344
DOI: 10.1039/C8SC04228D
COC(=O)CSc1cnc(NC(=O)N(C2CCCCC2)C2CCOCC2)s1
Reaction #197751
DOI: 10.1039/C8SC04228D
CN(C)S(=O)(=O)Cc1ccc2ccc3ncc(Cl)cc3c(=O)c2c1
Reaction #201705
DOI: 10.1039/C8SC04228D
COC(=O)C(C(C)C)S(=O)(=O)N(C)c1nc(OC)cc(OC)n1
Reaction #202175
DOI: 10.1039/C8SC04228D
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