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591179

Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
Reaction #2715
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)C1Cc2c(Br)ccc(OC)c2C1=O
Reaction #5446
white solid
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1C(O)=C(C(N)=O)C(=O)C2(O)C(O)=C3C(=O)c4c(O)ccc(Br)c4CC3CC12.O=S(=O)(O)O
Reaction #6539
pure product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)cc2c1OC(C)(C)CC2(C)C
Reaction #52397
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Br)ccc1O
Reaction #54103
18
Ausbeute 181.2%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(Br)cc1C(O)c1ccccc1
Reaction #54104
19
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1cc(CCC(=O)O)ccc1-c1ccc(-c2ccc(OCC(=O)O)c(Cc3cccc4ccccc34)c2CC(C)C)cc1
Reaction #54126
3-(4-(Carboxymethoxy)-2,2″-diisobutyl-3-naphthalen-1-ylmethyl-[1,1′:4′,1″]-terphenyl-4″-yl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(Br)cc1C(C)=O
Reaction #57573
(2-acetyl-4-bromo-phenoxy)-acetic acid ethyl ester
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)O)oc2ccc(Br)cc12
Reaction #57574
5-bromo-3-methyl-benzofuran-2-carboxylic acid
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #59025
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)ccc1OCC(=O)O
Reaction #59026
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)c1cc(Br)ccc1O2
Reaction #66751
tert-Butyl 6-bromo-4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccc3c(c2)C(=O)CC2(CCN(C(=O)OC(C)(C)C)CC2)O3)cn1
Reaction #66754
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)cc(F)c1O
Reaction #67276
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)cc(F)c1OCC1CO1
Reaction #67277
title compound
Ausbeute 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cc(Br)cc(F)c1OCC1CO1
Reaction #67278
crude title compound
Ausbeute 189.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)cc(F)c1OC[C@H]1CO1
Reaction #67282
title compound
Ausbeute 39.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Br)cc(Cl)c1OCC1CO1
Reaction #67302
title compound
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cc(Br)cc(Cl)c1OCC1CO1
Reaction #67303
crude title compound
Ausbeute 149.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(N2CCN(C)CC2)ccc1O
Reaction #74083
desired product
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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