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1123776

CSC(C)(C)C(=O)N[C@@H](CS)C(=O)O
Reaction #214478
titled compound
収率 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(C(=O)C(C)(C)S(=O)(=O)CC(Cc2ccccc2)C(=O)OCc2ccccc2)CC(C)O1
Reaction #288417
DOI: 10.1039/C8SC04228D
CC(C)(C(=O)Cl)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #362777
(RS)-2-[[2-[(Benzyloxy)carbonyl]-3-phenylpropyl]sulfonyl]-2-methylpropionyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(N)=O)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #362778
benzyl rac-α-[[(1-carbamoyl-1-methylethyl)sulfonyl]methyl]hydrocinnamate
収率 91.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)NC1CC1)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #362780
benzyl rac-α-[[[1-(cyclopropylcarbamoyl)-1-methylethyl]sulfonyl]methyl]hydrocinnamate
収率 86.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)OCC1CC1)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #362787
benzyl rac-α-[[[1-[(cyclopropylmethoxy)carbonyl]-1-methylethyl]sulfonyl]methyl]hydrocinnamate
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCOCCOC(=O)C(C)(C)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #362788
benzyl rac-α-[[[1-[[2-(2-ethoxyethoxy)ethoxy]carbonyl]-1-methylethyl]sulfonyl]methyl]hydrocinnamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)N1CCOCC1)S(=O)(=O)C[C@@H](Cc1ccccc1)C(=O)O
Reaction #362796
(S)-α-[[[1-methyl-1-(morpholinocarbonyl)ethyl]sulfonyl]methyl]hydrocinnamic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)N1CCSCC1)S(=O)(=O)C[C@@H](Cc1ccccc1)C(=O)O
Reaction #362804
(S)-α-[[[1-methyl-1-[(tetrahydro-4H-1,4-thiazin-4-yl)carbonyl]ethyl]sulfonyl]methyl]hydrocinnamic acid
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)C(C)(C)S(=O)(=O)C[C@@H](Cc2ccccc2)C(=O)O)CC1
Reaction #362805
(S)-α-[[[1-methyl-1-[(4-methyl-1-piperazinyl)carbonyl]ethyl]sulfonyl]methyl]hydrocinnamic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)C(C)(C)S(=O)(=O)CC(Cc2ccccc2)C(=O)OCc2ccccc2)C[C@H](C)O1
Reaction #362813
benzyl (RS)-α-[[[1-[(cis-2,6-dimethylmorpholino)carbonyl]-1-methylethyl]sulfonyl]methyl]hydrocinnamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)Cl)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #384834
DOI: 10.1039/C8SC04228D
CSC(C)(C)C(=O)N[C@@H](CSSC[C@H](NC(=O)C(C)(C)SC)C(=O)O)C(=O)O
Reaction #549837
titled compound
収率 83.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C(C)(C)S(=O)(=O)c1ccc2c(c1)nc(CC(C)(C)C)n2CC1CC1
Reaction #730885
title compound
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Cc1nc2cc(S(=O)(=O)C(C)(C)C(=O)NCCO)ccc2n1CC1CC1
Reaction #730886
title compound
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CSC(C)(C)C(=O)NC(CS)C(=O)O
Reaction #787180
DOI: 10.1039/C8SC04228D
CC(C)(Sc1ccncc1)C(=O)Cl
Reaction #891250
DOI: 10.1039/C8SC04228D
CC(C)(C)Cc1nc2cc(S(=O)(=O)C(C)(C)C(=O)NCCO)ccc2n1CC1CC1
Reaction #1303792
DOI: 10.1039/C8SC04228D
COC(=O)C(C(=O)C1(SCc2ccc(OC)cc2)CCN(OC)CC1)c1c(C)cc(C)cc1C
Reaction #1327451
DOI: 10.1039/C8SC04228D
Cl.O=C(Cl)C1(c2cccnc2)CCCCS1
Reaction #1350504
2-chloroformyl-2-(pyrid-3-yl)-tetrahydrothiopyran hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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