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26539

COc1ccc(S(=O)(=O)N2CCc3ccccc32)cc1OCCCOc1ccccc1
Reaction #2239
title compound
Rendimiento 86.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#Cc2cn(CCOc3ccccc3)c(C)n2)ccn1
Reaction #8968
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(CCOc3ccc(Cl)cc3)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43832
{5-[[2-(4-Chloro-phenoxy)-ethyl]-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(CCCOc3ccccc3)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43836
{5-[(4-Fluoro-benzenesulfonyl)-(3-phenoxy-propyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(c1ccccc1)(c1ccccc1)[C@H]1CCCN(CCOc2ccccc2)C1
Reaction #49678
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(CCCn2c(=O)ccc3ccc(OC)cc32)CCN(CCOc2ccccc2)CC1
Reaction #68123
ethyl 4-(3-(7-methoxy-2-oxo-1,2-dihydroquinolin-1-yl)propyl)-1-(2-phenoxyethyl)piperidine-4-carboxylate
Rendimiento 90.7%DOI: 10.6084/m9.figshare.5104873.v1
SCCCOc1ccccc1
Reaction #93699
3-phenoxypropanethiol
Rendimiento 61.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc(OCCCCOc2ccc(C(=O)c3ccccc3)cc2)cc1
Reaction #94458
crystals
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc(OCCCOc2ccc(C(=O)c3ccccc3)cc2)cc1
Reaction #94459
crystals
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(C(F)(F)F)Cn2c(nc(N3CCOCC3)cc2=O)N1CCOc1ccccc1
Reaction #159553
(S)-2-Methyl-7-morpholin-4-yl-1-(2-phenoxyethyl)-2-trifluoromethyl-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccc(OCCNC3CC3)cc2)cc1
Reaction #164874
N-[2-(biphenyl-4-yloxy)ethyl]cyclo-propanamine
Rendimiento 96.3%DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1sc(=N)n(CCOc2ccccc2)c1C
Reaction #165588
title compound
Rendimiento 50.6%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(OCCCN2CCC(C3Oc4ccccc4Cn4cccc43)CC2)cc1
Reaction #173299
DOI: 10.1039/C8SC04228D
BrCCCCCCCOc1ccccc1
Reaction #174377
DOI: 10.1039/C8SC04228D
O=C(c1ccc(O)cc1)c1ccc(OCCBr)cc1
Reaction #176770
DOI: 10.1039/C8SC04228D
COc1ccc2nccc(-n3cc4c(n3)CCC(NCCOc3ccccc3)C4)c2n1
Reaction #178551
DOI: 10.1039/C8SC04228D
COc1ccc([N+](=O)[O-])cc1CN1CC2(CCN(CCCOc3ccccc3)CC2)OC1=O
Reaction #181137
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(OCCCc2ccc(OCCCCOc3ccccc3)cc2)c(C=O)c1
Reaction #181441
DOI: 10.1039/C8SC04228D
ClCCCCOc1ccccc1
Reaction #183402
DOI: 10.1039/C8SC04228D
N#CC1CCCCN1CCCOc1ccccc1
Reaction #185188
DOI: 10.1039/C8SC04228D
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