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488573

CCCN(C)C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42344
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C)C(=O)c1cc(C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncco2)c1
Reaction #42345
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(N)=O)cc(-c2ncco2)c1
Reaction #42559
5-(1,3-oxazol-2-yl)-N3,N3-dipropylisophthalamide
Rendimiento 148.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2nc(C)co2)c1
Reaction #42563
methyl 3-[(dipropylamino)carbonyl]-5-(4-methyl-1,3-oxazol-2-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)O)cc(-c2nc(C)co2)c1
Reaction #42564
3-[(dipropylamino)carbonyl]-5-(4-methyl-1,3-oxazol-2-yl)benzoic acid
Rendimiento 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2nc(C)co2)c1
Reaction #42565
N1-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-5-(4-methyl-1,3-oxazol-2-yl)-N3,N3-dipropylisophthalamide
Rendimiento 26.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42571
methyl 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoate
Rendimiento 27.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42572
3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoic acid
Rendimiento 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncco2)c1
Reaction #42573
N1-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-5-(1,3-oxazol-2-yl)-N3,N3-dipropylisophthalamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncco2)c1
Reaction #42574
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42576
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42577
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncco2)c1
Reaction #42578
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42580
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncco2)c1
Reaction #42582
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1CCCN1C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #49225
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1
Reaction #49226
2-(tributylstannyl)oxazole
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1CCCN1C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #49227
title compound
Rendimiento 75.7%DOI: 10.6084/m9.figshare.5104873.v1
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