Recherche de Sous-structure

CCCCN(CCCC)CCO

COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCN)CC2O)c2ccc(OC)cc2)cc1
Reaction #49192
compound 65
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCNC(=O)OC3CCC4(C)C(=CCC5C4CCC4(C)C(C(C)CCCC(C)C)CCC54)C3)CC2O)c2ccc(OC)cc2)cc1
Reaction #49193
Compound 66
Rendement 90.5%DOI: 10.6084/m9.figshare.5104873.v1
C1CCNC1.NP([O-])ON1C(=O)c2ccccc2C1=O
Reaction #49202
compound 78
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCN3C(=O)c4ccccc4C3=O)CC2OC(=O)CCC(=O)O)c2ccc(OC)cc2)cc1
Reaction #49203
compound 79
Rendement 89.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1C(=O)N(CC(=O)OC(C)(C)C)[C@@H]1[C@@H](C)C(=S)c1ccccc1
Reaction #49985
(3S,4S)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4[(1R)-1-phenylthiocarbonylethyl]-1-(t-butyloxycarbonylmethyl)azetidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N(CC(=O)O)[C@@H]1[C@@H](C)C(=S)c1ccc(Cl)cc1
Reaction #49989
(3S,4S)-3-[(1R)-1-hydroxyethyl]-4-[(1R)-1-p-chlorophenylthiocarbonylethyl]-1-(carboxymethyl)azetidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H]1C(=O)N[C@H](C2Cc3ccccc3C2)C(=O)N1C(C(=O)O)c1ccc(F)cc1F
Reaction #73895
(2RS)-2-(2,4-difluorophenyl)-2-[(3R,6R)-3-(2,3-dihydro-1H-inden-2-yl)-6-isobutyl-2,5-dioxopiperazin-1-yl]-ethanoic acid
Rendement 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H]1C(=O)N[C@H](C2Cc3ccccc3C2)C(=O)N1[C@@H](C(=O)N(C)C)c1ccc(F)cc1F
Reaction #73896
(2R)-2-(2,4-difluorophenyl)-2-[(3R,6R)-3-(2,3-dihydro-1H-inden-2-yl)-6-isobutyl-2,5-dioxopiperazin-1-yl]-N,N-dimethylethanamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OC(=O)c4ccc([N+](=O)[O-])cc4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #83378
17-allyl-1,14-dihydroxy-23,25-dimethoxy-13,19,21,27-tetramethyl-12-[2-[4-(p-nitrobenzoyloxy)-3-methoxycyclohexyl]-1-methylvinyl]-11,28-dioxa-4-azatricylco[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93836
red-orange liquid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@]2(CN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]1CCCCN1C(C)C)C1CCCCC1)C(C)(C)C)C(C)(C)C21CCC1
Reaction #164443
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCCC[C@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)N1C[C@]2(C[C@H]1C(=O)O)C(C)(C)C21CCC1)C(C)(C)C)C1CCCCC1
Reaction #164444
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCc1ccc(OCCN(C[C@@H](O)[C@@H](O)CO)C[C@@H](O)[C@@H](O)CO)cc1
Reaction #168513
product 19
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(NCCCCc1ccc(OCCN(C[C@@H](O)[C@H](O)[C@H](O)CO)C[C@@H](O)[C@H](O)[C@H](O)CO)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168514
compound 23
Rendement 20.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN2CCC1CC2CCc1ccccc1
Reaction #176270
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Cl)c(Cl)c1)N1CCC(=O)N(C(CO)CCN2CCC3(CC3)C(O)C2)CC1
Reaction #176299
DOI: 10.1039/C8SC04228D
CC1C(=O)N(CCCC(=O)N2CCC3(CC3)C(O)C2)CCN1C(=O)Nc1ccc(C(F)(F)F)cc1
Reaction #176558
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCC(O)C(=O)N(CCCCCCCCCCCCCC)CC(O)CO
Reaction #178818
DOI: 10.1039/C8SC04228D
O=C1C2CCCC(O2)C(=O)N1CCCCN1CCN(c2cncc(Cl)n2)CC1
Reaction #187331
DOI: 10.1039/C8SC04228D
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