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16808

COC(=O)c1ccc(C)c2ccccc12
Reaction #11953
compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CBr)c2ccccc12
Reaction #11954
title compound
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)O)c2ccccc12
Reaction #78210
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O)c2ccccc12
Reaction #84208
4-methoxy-1-naphthoic acid
Ausbeute 55.0%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=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
O=C(NC(Cc1ccc(C(F)(F)F)cc1)C(O)c1ccc(F)c(F)c1)c1ccc(F)c2ccccc12
Reaction #177593
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1cccc(OC(F)(F)C(F)F)c1)C(O)c1cccc(Cl)c1)c1ccc(F)c2ccccc12
Reaction #177815
DOI: 10.1039/C8SC04228D
COCCn1c(C)c(C)sc1=NC(=O)c1ccc(F)c2ccccc12
Reaction #178862
DOI: 10.1039/C8SC04228D
COC(=O)C=Cc1ccc(C(=O)O)c2ccccc12
Reaction #196251
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1cccc(C(F)(F)F)c1)C(O)c1ccc(F)cc1)c1ccc(F)c2ccccc12
Reaction #208240
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1cccc(OC(F)(F)C(F)F)c1)C(O)c1ccc(Oc2ccccc2)cc1)c1ccc(F)c2ccccc12
Reaction #208477
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(C(=O)O)c2c(Br)cccc12
Reaction #214903
8-Bromo-naphthalene-1,4-dicarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(Cc1ccc(C(F)(F)F)cc1)C(O)c1cccc(F)c1)c1ccc(F)c2ccccc12
Reaction #232864
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(CO)c2ccccc12
Reaction #234912
DOI: 10.1039/C8SC04228D
CC(F)(F)c1cccc(CC(NC(=O)c2ccc(F)c3ccccc23)C(O)c2ccc(F)cc2)c1
Reaction #249614
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(CO)c2ccccc12
Reaction #250169
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1ccc(C(F)(F)F)cc1)C(O)c1ccc(Cl)nc1)c1ccc(F)c2ccccc12
Reaction #258040
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(CBr)c2ccccc12
Reaction #260695
DOI: 10.1039/C8SC04228D
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