Busqueda de Subestructura

Oc1cccc(Br)c1

COc1cc(Br)c2oc(/C=C/c3ccccc3Cl)cc2c1
Reaction #11247
( 859 )
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1c(O)cc(Br)cc1C(=O)O
Reaction #45791
compound
Rendimiento 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1c(O)cc(Br)c([N+](=O)[O-])c1C(=O)O
Reaction #45792
5-bromo-2-(2,2-dimethylpropionylamino)-3-hydroxy-6-nitrobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cccc(Br)c1
Reaction #50379
allyl 3-bromophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cccc(Br)c1
Reaction #50411
allyl 3-bromophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCOc1cccc(Br)c1
Reaction #64431
ethyl 4-(3-bromophenoxy)butyrate
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCOc1cccc(Br)c1
Reaction #65680
ethyl 3-(m-bromophenoxy)propionate
Rendimiento 52.9%DOI: 10.6084/m9.figshare.5104873.v1
O=COc1cc(Br)ccc1OC[C@@H]1CO1
Reaction #67266
5-BROMO-2-[(2S)-OXIRAN-2-YLMETHOXY]PHENYL FORMATE
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@@H]1COc2ccc(Br)cc2O1
Reaction #67267
crude title compound
Rendimiento 57.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1cc(OC)c(OC)c(OC)c1Br
Reaction #76361
product
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(Br)cc1Oc1ccccc1
Reaction #79866
title compound
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(C=O)c2)OC1(C)C
Reaction #79867
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #84841
product
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1N1CCOCC1)C/C(=C\c1cc(Br)cc(OC(F)(F)F)c1)C2=O
Reaction #90517
(E)-2-(3-bromo-5-(trifluoromethoxy)benzylidene)-6-methoxy-5-morpholino-2, 3-dihydro-1H-inden-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCOc1cccc(Br)c1
Reaction #171584
ethyl 4-(3-bromophenoxy)butanoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1cccc(Br)c1
Reaction #171585
4-(3-Bromophenoxy)butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCOc2cc(Br)ccc21
Reaction #171586
8-bromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one
Rendimiento 50.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2cc(Br)c(N)c(OCC3CC3)c2)CCCC1
Reaction #176586
DOI: 10.1039/C8SC04228D
COc1cc(Nc2ncn(Cc3ccc(Cl)cc3)n2)ccc1-n1cnc(C)c1
Reaction #180874
DOI: 10.1039/C8SC04228D
COc1cc(Br)cc(N2CCN(Cc3ccc(OC)c(OC)c3)C(CNS(=O)(=O)c3ccc(-n4ccnc4)cc3)C2)c1
Reaction #186204
DOI: 10.1039/C8SC04228D
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