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541805

Cc1ncc(-c2ccc(C(C)N3CCC(CCCO)(c4ccc(F)cc4)OC3=O)cc2)cn1
Reaction #237541
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccc(C(C)N3CCC(CCCO)(c4ccc(F)cc4)OC3=O)cc2)c(C)n1
Reaction #240300
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2cncnc2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #293888
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2ccncn2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #375738
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2ncccn2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #924497
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2cc(Cl)ncn2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1022239
DOI: 10.1039/C8SC04228D
CC(c1ccc(-c2ccc(C(F)(F)F)cn2)cc1)N1CCC(CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1023432
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)cc(C)n1
Reaction #1133327
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2cnccn2)cc1)N1CC[C@](CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1133352
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2ccc(C(F)(F)F)cn2)cc1)N1CC[C@](CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1133353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2ncccn2)cc1)N1CC[C@](CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1133356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)nn1
Reaction #1133357
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)cc(C)[n+]1[O-]
Reaction #1133365
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)n1
Reaction #1133368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)nc(C)n1
Reaction #1133369
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2ccncn2)cc1)N1CC[C@](CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1133370
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2cncnc2)cc1)N1CC[C@](CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1133371
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccc(-c2cccnn2)cc1)N1CC[C@](CCCO)(c2ccc(F)cc2)OC1=O
Reaction #1133374
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)cn1
Reaction #1133380
(R)-6-(4-fluorophenyl)-6-(3-hydroxypropyl)-3-((S)-1-(4-(2-methylpyrimidin-5-yl)phenyl)ethyl)-1,3-oxazinan-2-one
Ausbeute 44.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc([C@H](C)N3CC[C@](CCCO)(c4ccc(F)cc4)OC3=O)cc2)c(C)n1
Reaction #1133385
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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