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593314

CCCC(=O)c1ccc(Br)cc1F
Reaction #204814
DOI: 10.1039/C8SC04228D
OC(c1ccc(Br)cc1F)c1ccccc1C(F)(F)F
Reaction #206726
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CC=C(c2cc(F)c(Br)cc2F)CC1
Reaction #250669
DOI: 10.1039/C8SC04228D
CCOC(C(=O)NCc1ccc(C#N)cc1)c1c(F)cc(-c2ccccc2)cc1F
Reaction #251251
DOI: 10.1039/C8SC04228D
COc1cncc(-c2ccc(C(Oc3cc(-c4ccc(CC(NC(=O)OC(C)(C)C)C(=O)O)cc4)nc(N)n3)C(F)(F)F)c(F)c2)c1
Reaction #253914
DOI: 10.1039/C8SC04228D
CC(O)c1ccc(Br)cc1F
Reaction #271320
DOI: 10.1039/C8SC04228D
OC1(c2ccc(Br)cc2F)CCC1
Reaction #276865
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(Br)cc1F
Reaction #297583
DOI: 10.1039/C8SC04228D
—
Reaction #326815
liquid
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #326816
liquid
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1c2ccc(Br)cc2OC[C@@H]1Cc1ccccc1
Reaction #364631
(3S,4R)-3-benzyl-7-bromo-chroman-4-ol
Ausbeute 49.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #364632
white solid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(C(OC)C(=O)NCc3ccc(C#N)cc3)c(F)c2)cc1
Reaction #376091
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCOC(c2ccc(Br)cc2F)C1
Reaction #395598
DOI: 10.1039/C8SC04228D
CC(O)c1ccc(Br)cc1F
Reaction #406442
DOI: 10.1039/C8SC04228D
COC(=O)c1c[nH]c2cc(Cl)c(-c3ccc(C4(O)CCC4)c(F)c3)cc12
Reaction #425507
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #536436
liquid
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)c1ccccc1C(O)c1ccc(Br)cc1F
Reaction #562606
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)c1ccccc1C(=O)c1ccc(Br)cc1F
Reaction #562607
title product
Ausbeute 102.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(O)c1ccc(Br)cc1F
Reaction #587439
desired product
DOI: 10.6084/m9.figshare.5104873.v1
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