Substructure Search

2329

CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1021
desired product
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #251968
DOI: 10.1039/C8SC04228D
Cl.N[C@H]1Cc2ccccc2[C@H]1Oc1ccc(Cl)c(Cl)c1
Reaction #1052424
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1Cc2ccccc2[C@H]1Oc1ccc(Cl)c(Cl)c1.Cl
Reaction #1052425
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1Cc2ccccc2[C@H]1Oc1ccc(Cl)c(Cl)c1.Cl
Reaction #1052426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1292867
DOI: 10.1039/C8SC04228D
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1987347
desired product
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](N=[N+]=[N-])[C@H](Oc2ccc(Cl)c(F)c2)C1
Reaction #2366786
trans-(±)-3-azido-4-(4-chloro-3-fluorophenoxy)-1-methylpyrrolidine
Yield 89.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](N)[C@H](Oc2ccc(Cl)c(F)c2)C1
Reaction #2366787
trans-(±)-4-(4-chloro-3-fluorophenoxy)-1-methylpyrrolidin-3-amine
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(NC(=O)N2CCc3cnc(NC4CCOCC4)nc3C2)C(Oc2ccc(Cl)c(F)c2)C1
Reaction #2366788
2-(tetrahydro-pyran-4-ylamino)-5,8-dihydro-6H-pyrido[3,4-d]pyrimidine-7-carboxylic acid [4-(4-chloro-3-fluoro-phenoxy)-1-methyl-pyrrolidin-3-yl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #2481496
desired product
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1