Busqueda de Subestructura

37930

COc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1CC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3.[Cl-]
Reaction #712364
title compound
Rendimiento 99.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1CC(=O)OCC(=O)O.[Cl-]
Reaction #712365
title compound
Rendimiento 91.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1CC(=O)OCC(=O)OCC(=O)OC(C)(C)c1ccccc1.[Cl-]
Reaction #712367
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1CC(=O)OC1CCOC1=O.[I-]
Reaction #712368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(C)C)c(S(=O)(=O)[O-])c(C(C)C)c1.OCCc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
Reaction #747107
5-[4-(2-hydroxyethyl)phenyl]-dibenzothiophenium 2,4,6-triisopropylbenzenesulfonate
Rendimiento 101.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(C)C)c(S(=O)(=O)[O-])c(C(C)C)c1.OCCc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
Reaction #997169
5-[4-(2-hydroxy-ethyl)phenyl]dibenzothiophenium 2,4,6-triisopropylbenzene-sulfonate
Rendimiento 101.6%DOI: 10.6084/m9.figshare.5104873.v1
F[B-](F)(F)F
Reaction #1294746
DOI: 10.1039/C8SC04228D
OCCc1ccc(-[s+]2c3ccccc3c3ccccc32)cc1.[I-]
Reaction #1726668
5-[4-(2-hydroxyethyl)phenyl]dibenzothiophenium iodide
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
F[B-](F)(F)F.c1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
Reaction #1819892
S-phenyldibenzothiophenium fluoroborate
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)CC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)C(F)(F)S(=O)(=O)[O-].c1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
Reaction #1929035
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc(-[s+]2c3ccccc3c3ccccc32)cc1
Reaction #1929036
title compound
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-[s+]2c3ccccc3c3ccccc32)cc(C)c1O.[Br-]
Reaction #1929038
title compound
Rendimiento 17474.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(OC(=O)COc2c(C)cc(-[s+]3c4ccccc4c4ccccc43)cc2C)CCCC1.[Br-]
Reaction #1929039
title compound
Rendimiento 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)CC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)C(F)(F)S(=O)(=O)[O-].CCC1(OC(=O)COc2c(C)cc(-[s+]3c4ccccc4c4ccccc43)cc2C)CCCC1
Reaction #1929040
title compound
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(OC(=O)COc2c(C)cc(-[s+]3c4ccccc4c4ccccc43)cc2C)CCCC1.C[C@H](CCC(=O)OCCC(F)(F)C(F)(F)S(=O)(=O)[O-])[C@H]1CC[C@H]2[C@@H]3C(=O)CC4CC(=O)CC[C@]4(C)[C@H]3CC(=O)[C@]12C
Reaction #1929041
title compound
Rendimiento 80.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].CCC1(OC(=O)COc2c(C)cc(-[s+]3c4ccccc4c4ccccc43)cc2C)CCCC1
Reaction #1929042
title compound
Rendimiento 93.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O)cc1-[s+]1c2ccccc2c2ccccc21.[I-]
Reaction #1929043
title compound
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].CCC1(OC(=O)COC(=O)c2ccc(OC)c(-[s+]3c4ccccc4c4ccccc43)c2)CCCC1
Reaction #1929044
title compound
Rendimiento 86.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-[s+]2c3ccccc3c3ccccc32)cc(C)c1OCC(=O)OC(C)(C)c1ccccc1.[Br-]
Reaction #1929046
title compound
Rendimiento 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)CC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)C(F)(F)S(=O)(=O)[O-].Cc1cc(-[s+]2c3ccccc3c3ccccc32)cc(C)c1OCC(=O)OC(C)(C)c1ccccc1
Reaction #1929047
title compound
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
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