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1301688

C#Cc1cccc(Oc2ccc(C(=O)OC(=O)c3ccc(Oc4cccc(C#C)c4)c4ccccc34)c3ccccc23)c1
Reaction #55252
4-(3-ethynylphenoxy)naphthalic anhydride
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(Br)c2ccccc12
Reaction #92147
(4-bromonaphthalen-1-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(Br)c2ccccc12
Reaction #92148
4-bromonaphthalene-1-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #159002
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #166954
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2ccc3c4c(cccc24)COC3)CCN1
Reaction #186282
DOI: 10.1039/C8SC04228D
COC(=O)C=Cc1ccc(C(=O)O)c2ccccc12
Reaction #196251
DOI: 10.1039/C8SC04228D
O=C(O)c1c(Br)c(Br)c2c(Br)c(Br)ccc2c1C(=O)O
Reaction #216285
tetrabromonaphthalene-1,2-dicarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C=Cc2ccccc2)c2ccccc12
Reaction #258677
DOI: 10.1039/C8SC04228D
—
Reaction #304467
solid
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(Br)ccc(c23)C(=O)N1OCc1ccccc1
Reaction #366137
title compound
Ausbeute 87.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)ON1C(=O)c2cccc3c(Br)ccc(c23)C1=O
Reaction #366156
title compound
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(Br)ccc(c23)C(=O)N1O
Reaction #366172
title compound
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(Br)c2ccccc12
Reaction #441827
4-bromo-1-acetylnaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)c2ccccc12
Reaction #441828
naphthalene-1,4-dicarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Br)c2ccc(OS(C)(=O)=O)cc12
Reaction #499371
Methyl 4-Bromo-7-[(methanesulfonyl)oxy]naphthoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Br)c2ccc(O)cc12
Reaction #499372
titled product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Br)c2ccccc12
Reaction #504705
4-bromonaphthalene-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(CCCCCCC)N1C(=O)c2cccc3c(Br)ccc(c23)C1=O
Reaction #535902
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc(Br)c2ccccc12
Reaction #536308
(4-Bromo-naphthalen-1-yl)-phenyl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
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