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12484

CC(C)(Cc1c[nH]c2c(C=CS(C)(=O)=O)cccc12)NC(=O)OC(C)(C)C
Reaction #8204
{2-[7-(2-Methanesulfonyl-vinyl)-1H-indol-3-yl)-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(CCS(C)(=O)=O)cccc12)NC(=O)OC(C)(C)C
Reaction #8205
{2-[7-(2-methanesulfonyl-ethyl)-1H-indol-3-yl]-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCS(=O)(=O)c2cc(Nc3ncc4c(n3)N(C)C(=O)N(c3c(F)cccc3Br)C4)ccc21
Reaction #9829
title compound
Выход 31.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(CC1CNC1)c1ccccc1
Reaction #46339
3-(phenylsulfonylmethyl)azetidine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(S(=O)(=O)c2ccc3c(ccn3Cc3ccccc3)c2)n[nH]1
Reaction #51028
6-(N-Benzylindole-5-sulfonyl)-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)S(C)(=O)=O)s1
Reaction #53484
1-[bis(4-chlorophenyl)methyl]-3-[(methylsulfonyl)(2-methoxycarbonylthien-5-yl)methylene]azetidine
Выход 15.3%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C=C1CN(C(c2ccccc2)c2ccccc2)C1)Cc1cccc(OCCCCN2CCOCC2)c1
Reaction #53512
4-(4-{3-[(1-benzhydrylazetidin-3-ylidene)methanesulfonylmethyl]phenoxy}butyl)morpholine
DOI: 10.6084/m9.figshare.5104873.v1
CSC(NCCSCc1[nH]cnc1C)=C(C#N)S(=O)(=O)c1ccccc1
Reaction #55664
title product
DOI: 10.6084/m9.figshare.5104873.v1
C#CCNC(=CS(=O)(=O)c1ccccc1)NCCSCc1[nH]cnc1C
Reaction #55668
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C=C.CC(C)C[C@H](N)C(=O)O.Cc1ccc(S(=O)(=O)O)cc1
Reaction #60573
Leu Vinylsulfone Tosylate Salt
DOI: 10.6084/m9.figshare.5104873.v1
COCCOC/C(=C\S(=O)(=O)c1ccc(Cl)cc1)C(=O)OC(C)(C)C
Reaction #81738
oil
Выход 104.7%DOI: 10.6084/m9.figshare.5104873.v1
COCCOC/C(=C\S(=O)(=O)c1ccc(Br)cc1)C(=O)OC(C)(C)C
Reaction #81739
oil
Выход 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C=C(c1cc(Cl)cc(Cl)c1)C(F)(F)F)c1ccccc1
Reaction #90905
2-(3,5-dichlorophenyl)-3,3,3-trifluoroprop-1-en-1-yl phenyl sulfone
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C=C(c1cc(Cl)cc(Cl)c1)C(F)(F)F)c1ccccc1
Reaction #90906
2-(3,5-dichlorophenyl)-3,3,3-trifluoroprop-1-en-1-yl phenyl sulfone
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C(CCCCCCC(=O)O)CCCC(O)CCCCC
Reaction #93918
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C(CCCCCCC(=O)O)CCCC(O)CCCCC
Reaction #93919
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)c1cnc2c(F)cccc2c1O
Reaction #159822
4-hydroxy-3-phenylsulfonyl-8-fluoroquinoline
Выход 3.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(/C=C/S(=O)(=O)Cc2ccc(OC)c([N+](=O)[O-])n2)c(OC)c1
Reaction #159845
titled compound
Выход 35.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(/C=C/S(=O)(=O)Cc2ccc(OC)c(NS(C)(=O)=O)n2)c(OC)c1
Reaction #159846
title compound
Выход 5.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C(C#N)S(=O)(=O)c1ccccc1
Reaction #173418
DOI: 10.1039/C8SC04228D
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