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1124597

COC(=O)C1CC(Sc2ccccc2)C1C(=O)OC
Reaction #6068
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(S(=O)(=O)c2ccccc2)C1C(=O)OC
Reaction #6069
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCCCOS(=O)(=O)c1ccc(C)cc1
Reaction #43912
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1NCCSC1S(=O)(=O)c1ccc(Oc2ccc(-c3ccoc3)cc2)cc1
Reaction #51451
4-(4-(furan-3-yl)phenoxy)benzenesulfonyl-tetrahydro-2H-1,4-thiazine-3-carboxylic acid
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1NCCSC1S(=O)(=O)c1ccc(Oc2ccc(-c3ccoc3)cc2)cc1
Reaction #51452
4-(4-(furan-3-yl)phenoxy)benzenesulfonyl-tetrahydro-2H-1,4-thiazine-3-carboxamide
Выход 14.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #51503
( 4 )
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=CCC1C(=O)N2C(C(=O)OCc3ccccc3)=C(S(=O)c3ccccc3)CC12
Reaction #56016
benzyl 6-(3-methoxycarbonylprop-2-ene-1-yl)-7-oxo-3-phenylsulphinyl-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
Выход 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(Sc2ccccc2)C1C(=O)OCc1ccc(F)c(Oc2ccccc2)c1
Reaction #56378
4-fluoro-3-phenoxybenzyl 3-phenylthio-2,2-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccc(F)c(Oc2ccccc2)c1)C1C(Sc2ccccc2)C1(Cl)Cl
Reaction #56379
4-fluoro-3-phenoxybenzyl 3-phenylthio-2,2-dichlorocyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1SC[C@@H](NC(=O)OCc1ccccc1)C(=O)O
Reaction #81399
S-(o-aminophenyl)-N-carbobenzyloxy-D-cysteine
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CSc2ccccc2NC1=O)OCc1ccccc1
Reaction #81400
3(S)-[(Carbobenzyloxy)amino]-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=CCC1C(=O)N2C(C(=O)OCc3ccccc3)=C(S(=O)c3ccccc3)CC12
Reaction #96212
benzyl 6-(3-methoxycarbonylprop-2-ene-1-yl)-7-oxo-3-phenylsulphinyl-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
Выход 93.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCS(=O)c1ccc(Cl)cc1NS(=O)(=O)c1ccc(Cl)cc1F
Reaction #157655
title compound
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCCSc1ccc(Br)cc1
Reaction #157763
title compound
Выход 95.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/C2CCCC2)c2ccc(SCCCOS(=O)(=O)c3ccc(C)cc3)c(Cl)c2)nc1OC
Reaction #157775
3-({2-chloro-4-[(E)-2-cyclopentyl-1-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]phenyl}sulfanyl)propyl 4-methylbenzenesulfonate
Выход 93.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/C2CCCC2)c2ccc(SCCCN(CC)CC)c(Cl)c2)nc1OC
Reaction #157776
3-({2-chloro-4-[(E)-2-cyclopentyl-1-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]phenyl}sulfanyl)-N,N-diethylpropan-1-amine
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)SCCN(S(=O)(=O)c2ccc3ccccc3c2)C1C(=O)O
Reaction #164517
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCOS(C)(=O)=O)S(=O)(=O)c1ccccc1
Reaction #175637
DOI: 10.1039/C8SC04228D
CC(=O)C=CCCSc1ccc(C(F)(F)F)cc1
Reaction #175852
DOI: 10.1039/C8SC04228D
CC(=O)N1CCC(c2csc(Nc3ncc(SCCCO)cc3Oc3ccccc3)n2)CC1
Reaction #188308
DOI: 10.1039/C8SC04228D
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