4-fluoro-benzyl bromide

Fc1ccc(COc2cc3ccc(Br)cc3cc2C23CC4CC(CC(C4)C2)C3)cc1
Reaction #1238
expected compound
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(=O)[C@@H]1CCCC[C@@H]1N(Cc1ccc(F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7134
titled compound
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(F)cc1
Reaction #7511
title compound
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)Nc1nc2ccc(Br)c(OCc3ccc(F)cc3)c2s1
Reaction #9212
desired compound 13
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)c1cccn1Cc1ccc(F)cc1
Reaction #11328
2-acetyl-1-(4-fluorobenzyl)pyrrole
収率 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=c1cc(OCc2ccc(F)cc2)ccn1-c1ccc(OCCN2CCCCC2)cn1
Reaction #43319
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CCOc1ccc(-n2ccc(OCc3ccccn3)cc2=O)cc1
Reaction #43338
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3Cc2ccc(F)cc2)CC1
Reaction #48122
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(COc2cc(-c3ccccc3)nc(-c3ccncc3)n2)cc1
Reaction #58176
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Fc1ccc(COc2nc(-c3ccccc3)nc3c2CCC3)cc1
Reaction #58177
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Fc1ccc(COc2cc(-c3ccccc3)nc(-c3ccc(Cl)cc3)n2)cc1
Reaction #58178
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1cc(OCc2ccc(F)cc2)nc(-c2cc(Cl)cc(Cl)c2)n1
Reaction #58181
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Fc1ccc(COc2nc(-c3cc(Cl)cc(Cl)c3)nc3c2CN(Cc2ccccc2)CC3)cc1
Reaction #58182
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)c1cc(OCc2ccc(F)cc2)nc(-c2cccc([N+](=O)[O-])c2)n1
Reaction #58183
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1cccc(C(=O)N2CCC(c3cn(Cc4ccc(F)cc4)c4ccccc34)CC2)c1
Reaction #70512
3-{4-[1-(4-Fluoro-benzyl)-1H-indol-3-yl]-piperidine-1-carbonyl}-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(=O)N1CCC(N(Cc2ccc(F)cc2)C(=O)OC(C)(C)C)CC1
Reaction #78072
O-tert-butyl N-(4-fluorobenzyl)-N-(1-acetylpiperidin-4-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Fc1ccc(Cc2ccco2)cc1
Reaction #80442
2-(4-fluorophenylmethyl)furan
収率 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Fc1ccc(Cc2cccs2)cc1
Reaction #80451
2-(4-fluorophenylmethyl)thiophene
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Fc1ccc(Cc2cccs2)cc1
Reaction #80456
2-(4-fluorobenzyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Fc1ccc(COCc2cccs2)cc1
Reaction #80463
2-(4-fluorophenylmethoxymethyl)thiophene
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
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