Поиск подструктуры

1402859

N#Cc1ccc(OC(F)F)cc1
Reaction #3113
title compound
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OC(F)F)cc1
Reaction #3114
title compound
Выход 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CCO[Si](OCC)(OCC)OC(=O)C(F)(F)Cl
Reaction #12079
chlorodifluoroacetic acid, triethoxysilyl ester
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1ccc(Br)nc1
Reaction #43322
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
OC(=S)CCc1ccc(F)cc1
Reaction #55088
said acid
Выход 90.6%DOI: 10.6084/m9.figshare.5104873.v1
OC(=S)CCc1ccc(Cl)cc1Cl
Reaction #55090
product
Выход 88.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC(O)=S)cc1OC
Reaction #55093
3,4-Dimethoxybenzylthio-acetic acid
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
OC(=S)CCc1ccc(F)cc1
Reaction #56457
said acid
Выход 90.6%DOI: 10.6084/m9.figshare.5104873.v1
OC(=S)CCc1ccc(Cl)cc1Cl
Reaction #56459
product
Выход 88.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCC(O)=S)cc1OC
Reaction #56462
3,4-Dimethoxybenzylthio-acetic acid
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1cccnc1Cl
Reaction #67630
2-chloro-3-(difluoromethoxy)pyridine
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1cnc2c(NCc3nnc4ccc(-c5ccccc5)nn34)ccnc2c1
Reaction #68538
title compound
Выход 17.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc3nnc(COc4ccnc5cc(OC(F)F)ccc45)n3c2)on1
Reaction #68611
7-(difluoromethoxy)-4-((6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)quinoline
Выход 13.4%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1cnc2c(Cl)ccnc2c1
Reaction #68647
8-chloro-3-(difluoromethoxy)-1,5-naphthyridine
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC(F)F)cnc1C#N
Reaction #168794
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc(OC(F)F)cc1Cl
Reaction #168802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cc(Cc3ccc(OC(F)F)nc3)c3ccccc3c2ncn1[C@H]1CCOC[C@@H]1O
Reaction #169645
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1n(-c2ccc(OCc3ccccc3)cc2)c2ncccc2n1C(F)F
Reaction #169779
3-[4-(benzyloxy)phenyl]-1-(difluoromethyl)-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
Выход 18.1%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(-c2ccc(OCc3ccccc3)cc2)c2ncc(OC(F)F)cc21
Reaction #169840
3-[4-(benzyloxy)phenyl]-6-(difluoromethoxy)-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
Выход 32.2%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OC(F)F)nc1
Reaction #304459
2-difluoromethoxy-5-nitro-pyridine
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
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