Recherche de Sous-structure

C(CCS)CO

O=C(O)CCCS(=O)(=O)c1cn(CC(=O)O)c2c(/C=C/c3ccc(OCCCCOc4ccccc4)cc3)cccc12
Reaction #40906
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCC2(O)CCS(=O)(=O)CC2)cc(C)c1-c1cccc(COc2ccc3c(c2)OC[C@H]3CC(=O)O)c1
Reaction #43945
title compound
Rendement 76.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(SC[C@@H]2C[C@H](CC(=O)OC(C)(C)Cc3ccccc3)OC(C)(C)O2)nc2ccccc21
Reaction #67682
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(N(C)S(C)(=O)=O)nc(-c2ccc(F)cc2)c1/C=C/[C@@H]1C[C@H](CC(=O)OC(C)(C)Cc2ccccc2)OC(C)(C)O1
Reaction #67684
title compound
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2CO[C@@H](COS(=O)(=O)c3ccc(C)cc3)[C@@H]2O)cc1
Reaction #83102
desired product
Rendement 57.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2CO[C@@H](CN=[N+]=[N-])[C@@H]2O)cc1
Reaction #83103
desired product
Rendement 32.6%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(NC(=O)c4ccccc4)=N[C@@]3(c3cc(C#N)ccc3F)CO2)cn1
Reaction #155610
N-[(4aR,6R,8aS)-8a-(5-cyano-2-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(C#N)ccc3F)CO2)cn1
Reaction #155611
product
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](C)NCc1ccc(F)c([C@]23CO[C@@H](c4cnn(C)c4)C[C@H]2CSC(N)=N3)c1
Reaction #155619
product
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc([C@H]2OC3(CC[C@H](CSc4nnnn4-c4ccccc4)C3)O[C@@H]2c2ccccc2)cc1
Reaction #157700
5-({[(2R,3R,7S)-2,3-diphenyl-1,4-dioxaspiro[4.4]non-7-yl]methyl}sulfanyl)-1-phenyl-1H-tetrazole
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C\[C@H]2CCC3(C2)O[C@H](c2ccccc2)[C@@H](c2ccccc2)O3)c2ccc(C3CC3)c(OC)n2)cc1
Reaction #157782
3-cyclopropyl-6-[(E)-2-[(2R,3R,7S)-2,3-diphenyl-1,4-dioxaspiro[4.4]non-7-yl]-1-(4-ethylphenyl)ethenyl]-2-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1
CSCC1C2OC(C)(C)OC2C(c2c[nH]c(C#N)c2N)N1C(=O)OC(C)(C)C
Reaction #178043
DOI: 10.1039/C8SC04228D
CC1(C)Oc2ccc(Cl)cc2C(CS(=O)(=O)NCC(=O)NCCc2ccccc2)C1O
Reaction #179965
DOI: 10.1039/C8SC04228D
O=C(O)CCCSc1ccc(C23CC4CC(CC(C4)C2)C3)cc1
Reaction #180295
DOI: 10.1039/C8SC04228D
CC12COC(CCCC=CCC3C(O)CC(O)C3CS(=O)(=O)c3ccccc3)(OC1)OC2
Reaction #185166
DOI: 10.1039/C8SC04228D
COC(=O)C1(CSC(C)=O)CCOCC1
Reaction #198359
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2SCCC1(CO)COC(=S)Nc1cccc2ccccc12
Reaction #199179
DOI: 10.1039/C8SC04228D
COC1C(O)CCC(O)(CSc2ccccc2)C1C1(C)OC1CC=C(C)C
Reaction #201751
DOI: 10.1039/C8SC04228D
C=C(CC1COC(C)(C)O1)S(=O)(=O)Nc1c(OC)cc(F)c(F)c1Nc1ccc(I)cc1F
Reaction #207695
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc2ccccc2c1)N1CC(COCc2ccccc2)C(CSC(c2ccccc2)(c2ccccc2)c2ccccc2)C1
Reaction #223251
DOI: 10.1039/C8SC04228D
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