بحث البنية الفرعية

CCCCCCCCCCN(C)C

CNCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl.Cl
Reaction #11560
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCN(CC=O)C(=O)OCC1c2ccccc2-c2ccccc21
Reaction #41717
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CNCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl.Cl
Reaction #46680
1-[2-(1-Adamantyl)ethyl]-1-(2-methylaminoethyl)-3-[3-(4-pyridyl)propyl]urea dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48643
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49205
Compound 83
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCCCCCCCN1CCOCC1
Reaction #50079
12-morpholinyldodecylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@H](CCCCCN(CCO)CCO)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53892
trans-N-(4-{5-[Bis-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCC[C@H]1CC[C@H](N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #53902
trans-{4-[4-(Allyl-methyl-amino)-butyl]-cyclohexyl}-methyl-carbamic acid 4-chloro-phenyl ester
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)CCCCC[C@H]1CC[C@H](NS(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53930
trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-4-trifluoromethyl-benzenesulfonamide
المردود 80.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53942
trans-5-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyl}-pentanoic acid diethylamide
المردود 85.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CC(c2cccc3ccccc23)C2CCCCCCC2O)CC1.Cl.Cl
Reaction #57113
2-(4-methylpiperazin-1-yl-1-(1-naphthyl)ethyl]cyclooctanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
OCCCCCCCCCCCN1CCCCC1
Reaction #65038
1-hydroxy-11-(N-piperidyl)undecane
المردود 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCN(CC=O)C(=O)OCC1c2ccccc2-c2ccccc21
Reaction #72417
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)N[C@@H](CCCCNC(=O)CCCCCCCCCCN(Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #84607
(19S,23S)-tri-tert-butyl 1-(1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)-2-((1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)methyl)-13,21-dioxo-2,14,20,22-tetraazapentacosane-19,23,25-tricarboxylate
المردود 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)c1cc(NS(=O)(=O)c2ccc(S(=O)(=O)CCC#N)cc2)c2ccccc2c1O
Reaction #95993
tan solid
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCN(CCCN)CCCN
Reaction #161894
target compound
المردود 103.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)N[C@@H](CCCCNC(=O)CCCCCCCCCCN(Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)Cc1nccn1CC(=O)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #164800
(19S,23 S)-tri-tert-butyl 1-(1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)-2-((1-(2-(bis(2-tert-butoxy-2-oxoethyl)amino)-2-oxoethyl)-1H-imidazol-2-yl)methyl)-13,21-dioxo-2,14,20,22-tetraazapentacosane-19,23,25-tricarboxylate
المردود 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)C1CCC(O)CC1CC1OC(C)(C)N(C(=O)OC(C)(C)C)C1Cc1ccccc1
Reaction #173153
DOI: 10.1039/C8SC04228D
C=CCOC(=O)N1CCC(C(=O)CC2NC(=O)C2C(CO[SiH](C)C)C(C)(C)C)C1
Reaction #188942
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCC(=O)N(C)CCOC(=O)c1ccc(C)cc1
Reaction #190883
DOI: 10.1039/C8SC04228D
الصفحة 1التالي