Busqueda de Subestructura

16120

O=C(NCc1ccc(Br)cc1F)OCc1ccccc1
Reaction #1300
O-benzyl N-(4-bromo-2-fluorobenzyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C=Cc2ccc(Br)cc2)cc1
Reaction #7291
desired product
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(Br)cc1F
Reaction #7794
4-bromo-2-fluoro benzyl cyanide
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(Br)cc1F
Reaction #7796
4-bromo-2-fluoro benzyl cyanide
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(Br)cc1F
Reaction #7798
4-bromo-2-fluoro benzyl cyanide
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(Br)cc1F
Reaction #7800
4-bromo-2-fluoro benzyl cyanide
DOI: 10.6084/m9.figshare.5104873.v1
[NH4+].[OH-]
Reaction #50828
NH4OH
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52513
EtOAc—hexanes
Rendimiento 2.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1Cn1ccnc1
Reaction #52514
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(C(=O)OC)ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64562
title compound
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64566
title compound
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(Br)cc1F
Reaction #64571
title compound
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC1=CC(=O)C(Cc2ccc(Br)cc2)C1
Reaction #69413
5
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(CN(Cc2ccc(Br)cc2)c2ccc3[nH]cnc3c2)cc1
Reaction #74223
N,N-Bis(4-bromobenzyl)-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)cc(Oc2cc(Br)ccc2CBr)c1
Reaction #76287
bromide
Rendimiento 224.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](OCc2ccc(Br)cc2)C[C@H]1C(=O)O
Reaction #78246
trans-N-Boc-4-(4-bromo-benzyloxy)-L-proline
Rendimiento 30.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](OCc2ccc(Br)cc2)C[C@@]1(C)C(=O)O
Reaction #78257
(2S,4R)-N-Boc-4-(4-bromo-benzyloxy)-2-methyl-proline
Rendimiento 28.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(c2cc(Cl)cc(Cl)c2)C(=O)C2(Cc3ccc(Br)cc3)Cc3ccccc3CN12
Reaction #78265
compound
Rendimiento 66.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #80079
EtOAc-hexanes
Rendimiento 2.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1Cn1ccnc1
Reaction #80080
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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