Поиск подструктуры

1336824

CNC(=O)C(Br)CCBr
Reaction #181268
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(OCc2ccccc2)cc1)C(Br)CCBr
Reaction #289850
DOI: 10.1039/C8SC04228D
CC(C)N1OCCC(Br)C1=O
Reaction #416778
dihydro-4-bromo-2-isopropyl-2H-1,2-oxazin-3(4H)-one
Выход 10.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)C(CCBr)OC(C#CC3CC3)(C(F)(F)F)c3cc(Cl)ccc32)cc1
Reaction #456929
title compound
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNC(=O)C(Br)CCBr
Reaction #669667
rac-2,4-Dibromo-N-isobutyl-butyramide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(Br)CCBr
Reaction #687714
product
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(Br)ccc1N1CCC(Br)C1=O
Reaction #792680
3-bromo-1-(6-bromo-2-methylpyridin-3-yl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #803105
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCC(Br)C2=O)ccc1Cl
Reaction #809163
title compound
Выход 43.3%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCC(Br)C1=O
Reaction #1196468
objective compound
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCC(Br)C1=O
Reaction #1196534
objective compound
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCC(Br)C1=O
Reaction #1219698
DOI: 10.1039/C8SC04228D
O=C(OCc1ccccc1)c1ccccc1N1CCC(Br)C1=O
Reaction #1461257
(3-Bromo-2-oxo-pyrrolidin-1-yl)benzoic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(C(F)(F)F)ccn1)C(Br)CCBr
Reaction #1466462
title compound
Выход 83.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)C(Br)CCBr)cc1F
Reaction #1594352
2,4-dibromo-N-(3-fluoro-4-methylbenzyl)butanamide
Выход 87.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCC(Br)C2=O)cc1F
Reaction #1594414
racemic 3-bromo-1-(3-fluoro-4-methylphenyl)pyrrolidin-2-one
Выход 54.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(Br)CCBr)c1ccc(F)cc1
Reaction #1594416
2,4-Dibromo-N—((S)-1-(4-fluorophenyl)ethyl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(C(F)(F)F)cc1)C(Br)CCBr
Reaction #1594432
2,4-dibromo-N-(4-(trifluoromethyl)benzyl)-butanamide
Выход 94.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1OCCC(Br)C1=O
Reaction #1673873
4-Bromotetrahydro-2-methyl-2H-1,2-oxazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1(Br)SC=C(Br)C1Br)C(=O)O
Reaction #1821887
N-(2',3',4'-tribromothenoyl)-L-alanine
Выход 60.4%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее