Busqueda de Subestructura

CC(Cl)(Cl)Cl

COc1cccc2[nH]cc(C(=O)C(Cl)(Cl)Cl)c12
Reaction #998
4-methoxy-3-trichloroacetyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #1859
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(Cl)(Cl)Cl)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41322
2,2,2-Trichloro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1csc(Br)n1)C(Cl)(Cl)Cl
Reaction #54479
title compound
Rendimiento 53.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N(C(=O)Nc1nc(C(Cl)(Cl)Cl)ns1)c1ccccc1
Reaction #56274
pure product
Rendimiento 24.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccsc1NC(=O)NC(=O)C(Cl)(Cl)Cl
Reaction #58622
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)sc1NC(=O)NC(=O)C(Cl)(Cl)Cl
Reaction #58623
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #82192
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2nc(C(Cl)(Cl)Cl)[nH]c2c1
Reaction #84894
6-Nitro-2-(trichloromethyl)-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2ccc(Cl)c(OCCOC3CCCCO3)c2)n1
Reaction #88920
title compound
Rendimiento 101.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2ccc(Cl)c(OCCCOC3CCCCO3)c2)n1
Reaction #88960
title compound
Rendimiento 70.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CCCN1c1nnc2ccc(O[C@@H]3CC[C@H](NC(=O)Nc4cc(C(C)(C)C)nn4-c4ccc(Cl)c(OCCOC5CCCCO5)c4)c4ccccc43)cn12
Reaction #88963
title compound
Rendimiento 19.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(Cl)(Cl)Cl)Oc1cc2occ(C(=O)Cl)c(=O)c2cc1OC(=O)OCC(Cl)(Cl)Cl
Reaction #95376
6,7-Bis(2,2,2-trichloroethoxycarbonyloxy)chromone-3-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2cccc(CN3CCC(F)(F)CC3)c2)n1
Reaction #162769
title compound
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)OCC(Cl)(Cl)Cl)n(-c2ccc3cn(CCN4CCOCC4)nc3c2)n1
Reaction #162793
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CSC(C)c1ccc(C(Cl)(Cl)Cl)nc1
Reaction #169512
5-[1-(methylthio)ethyl]-2-(trichloromethyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc(C(Cl)(Cl)Cl)nc1)/S(C)=N/C#N
Reaction #169513
(1E)-methyl{1-[6-(trichloromethyl)pyridin-3-yl]ethyl}-sulfanylidenecyanamide
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(OC(c1ccccc1)c1ccc(Br)cc1)C(Cl)(Cl)Cl
Reaction #181471
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)c(C(F)(F)F)c1)C(Cl)(Cl)Cl
Reaction #183152
DOI: 10.1039/C8SC04228D
CC(=O)C(=NOCC(=O)OCC(Cl)(Cl)Cl)C(=O)OC(C)(C)C
Reaction #183281
DOI: 10.1039/C8SC04228D
Página 1Siguiente