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681077

CCOC(=O)C(C)(C)Oc1cccc(F)c1
Reaction #84552
title compound
Ausbeute 47.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Oc1cccc(F)c1)C(=O)O
Reaction #84553
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(Cl)c(F)c2)CCCn2c(-c3ccc(-n4cnc(C)c4)c(OC)n3)nnc21
Reaction #158264
title compound
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(Cl)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158309
title compound
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158339
title compound
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158340
title compound
Ausbeute 44.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCCC3(Oc2cc(F)c(F)c(F)c2)C(C)(C)O)ccc1-c1cnc(C)o1
Reaction #158341
title compound
Ausbeute 117.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158350
title compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(CC)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158352
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCNC1=O
Reaction #158354
title compound
Ausbeute 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCNC1=S
Reaction #158355
ethyl (3S)-2-thioxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylate
Ausbeute 142.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCN=C1SC
Reaction #158356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158357
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCC[C@]3(Oc2cc(F)c(F)c(F)c2)C(C)(C)O)ccc1-c1cnc(C)o1
Reaction #158358
title compound
Ausbeute 129.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCn2c(-c3ccc(-n4cnc(C)c4)c(OC)n3)nnc21
Reaction #158367
title compound
Ausbeute 41.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-n4cnc(C)c4)c(OC)n3)nnc21
Reaction #158368
title compound
Ausbeute 49.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)cc(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158370
title compound
Ausbeute 38.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(Oc2cc(F)c(F)c(F)c2)CCCn2c(-c3ccc(-n4cnc(C)c4)c(OC)n3)nnc21
Reaction #158372
title compound
Ausbeute 95.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCN(Cc2ccc(OC)cc2)C1=O
Reaction #158387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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