Substructure Search

1432191

Cc1ccc2cc(Br)ccc2c1
Reaction #59834
aimed compound
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc2cc(Br)ccc2c1
Reaction #59836
aimed compound
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3cc(Br)ccc3c2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #752851
DOI: 10.1039/C8SC04228D
Cc1ccc2cc(Br)ccc2c1
Reaction #757327
DOI: 10.1039/C8SC04228D
CC1CCCN1CCc1ccc2cc(Br)ccc2c1
Reaction #944712
1-[2-(6-bromo-naphthalen-2-yl)-ethyl]-2-methyl-pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN1CCc1ccc2cc(Br)ccc2c1
Reaction #944713
1-[2-(6-bromo-naphthalen-2-yl)-ethyl]-2-methyl-pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc2cc(Br)ccc2c1
Reaction #944716
product
Yield 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN1CCc1ccc2cc(Br)ccc2c1
Reaction #1026894
DOI: 10.1039/C8SC04228D
COC1OC(=O)c2ccc3cc(Br)ccc3c21
Reaction #1149065
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc2cc(Br)ccc2c1
Reaction #1624881
DOI: 10.1039/C8SC04228D
O=S(=O)(Oc1ccc2cc(Br)ccc2c1)C(F)(F)F
Reaction #2079101
title compound
Yield 101.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3cc(Br)ccc3c2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #2079102
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3cc(Br)ccc3c2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #2079103
title compound
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cc(Br)ccc2c1
Reaction #2199551
aimed compound
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc2cc(Br)ccc2c1
Reaction #2199553
aimed compound
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Oc1ccc2cc(Br)ccc2c1)C(F)(F)F
Reaction #2209925
DOI: 10.1039/C8SC04228D
C=Cc1ccc2cc(Br)ccc2c1
Reaction #2213072
DOI: 10.1039/C8SC04228D
CC1CCCN1CCc1ccc2cc(Br)ccc2c1
Reaction #2238432
DOI: 10.1039/C8SC04228D