Teilstruktursuche

830550

COC(=O)c1cc(N2CCOCC2)c(OC)cc1Cl
Reaction #512
Ausbeute 79.9%
COC(=O)c1cc(N2CCOCC2)c(OC)cc1Cl
Reaction #513
Ausbeute 54.4%
COC(=O)c1cc(N2CCOCC2)c(OC)cc1Cl
Reaction #514
Ausbeute 78.7%
CCCCN1CCOc2c(I)cc(C(=O)OC)cc21
Reaction #42465
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(-c3ncco3)cc(C(=O)OC)cc21
Reaction #42466
title compound
Ausbeute 71.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(-c3ncco3)cc(C(=O)O)cc21
Reaction #42467
title compound
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(-c3ncco3)cc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42468
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(Br)cc(C(=O)OC)cc21
Reaction #42471
Methyl 8-bromo-4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(C#N)cc(C(=O)OC)cc21
Reaction #42472
title compound
Ausbeute 66.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(C#N)cc(C(=O)O)cc21
Reaction #42473
title compound
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(C#N)cc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42474
title compound
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1C(=O)COc2ccc(C(=O)OC)cc21
Reaction #42495
phenoxazine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2ccc(C(=O)OC)cc21
Reaction #42496
title compound
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2ccc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42498
title compound
Ausbeute 17.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2c(c1)N1CCC[C@@H](NC(=O)C(F)(F)F)[C@H]1c1ccccc1O2
Reaction #44455
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OCCCCl)c(N(C)C)c1
Reaction #83877
black oily liquid
Ausbeute 179.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)N(C(=O)C(F)(F)F)CCO2)c1cc(Br)ccc1Cl
Reaction #159747
1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCOc2ccc(Cc3cc(Br)ccc3Cl)cc21)C(F)(F)F
Reaction #159748
1-[6-(5-bromo-2-chloro-benzyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)N(C(=O)C(F)(F)F)CCO2)c1cc(Br)ccc1Cl
Reaction #159753
1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCOc2ccc(Cc3cc(Br)ccc3Cl)cc21)C(F)(F)F
Reaction #159754
1-[6-(5-bromo-2-chloro-benzyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
Ausbeute 85.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter