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CC(C)CCO

N[C@@H]1CC[C@@H](c2cccc(F)c2F)C(CO)NC1=O
Reaction #48450
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(CO)[C@H](c2cccc(F)c2F)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48451
title compound
Выход 15.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)C(C)Oc1ccc(Oc2ccc(C#N)cc2)cc1
Reaction #63424
desired compound
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](N)C(=O)OC1CCC(n2cc(-c3ccc(Oc4ccccc4)cc3)c3c(N)ncnc32)C1.Cl
Reaction #79792
3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl (2S)-2-amino-3-methylbutanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(C(=O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)C=CC1CCO
Reaction #81618
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C=O)c1ccc(C(=O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)cc1
Reaction #81619
4-[4-[4-(hydoxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-α,α-dimethylbenzeneacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
N#N.NC(=O)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C[C@@]1(C(N)=O)CCCN1c1ccccc1
Reaction #82343
N2 [3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -phenyl-L-prolinamide
Выход 42.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@@H](N)Cc1ccccc1)C(N)=O.N#N
Reaction #82373
N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide
Выход 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1C[C@@H](O)C[C@@]1(C[C@@H](O)[C@@H](N)Cc1ccccc1)C(N)=O.N#N
Reaction #82386
N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-4(S)-hydroxy-L-prolinamide
Выход 98.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)OC(C)CC(C)(C)OOC(C)(C)C
Reaction #94251
1,3-Dimethyl-3-(t-butylperoxy)butyl n-butyl carbonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(CC(C)(C)OOC(C)(C)C)OC(=O)N(C)C
Reaction #94253
1,3-Dimethyl-3-(t-butylperoxy)butyl N,N-dimethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc([C@H]2C[C@H]3CSC(NC(=O)c4ccccc4)=N[C@@]3(c3cc(Br)ccc3F)CO2)n1
Reaction #155603
N-[(4aR,6R,8aS)-8a-(5-bromo-2-fluorophenyl)-6-(4-methyl-1,3-oxazol-2-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc([C@H]2C[C@H]3CSC(NC(=O)c4ccccc4)=N[C@@]3(c3cc(C#N)ccc3F)CO2)n1
Reaction #155604
N-[(4aR,6R,8aS)-8a-(5-cyano-2-fluorophenyl)-6-(4-methyl-1,3-oxazol-2-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(C#N)ccc3F)CO2)n1
Reaction #155605
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OC(C)(C)C)C1CC1CCO
Reaction #157673
title compound
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C1CCN(Cc2ccccc2)C1
Reaction #178495
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCOCC2NC(=O)c2ccccc2)CC1c1ccc(Cl)c(Cl)c1
Reaction #181391
DOI: 10.1039/C8SC04228D
O=C(O)C(F)(F)F
Reaction #187388
DOI: 10.1039/C8SC04228D
CC(C=CC=O)C1(C)CCC(C(O[SiH](c2ccccc2)c2ccccc2)C(C)(C)C)C1(C)C
Reaction #188991
DOI: 10.1039/C8SC04228D
COc1ccccc1C(C)C(=O)N1CC2CC(CC#N)CC(O)(c3ccccc3OC)C2C1
Reaction #194868
DOI: 10.1039/C8SC04228D
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