Teilstruktursuche

920534

COC(=O)[C@H](CC(C)C)N1CC(Oc2cccc3c2CCCC3)=CC1=O
Reaction #47339
(S)-4-methyl-2-[2-oxo-4-(5,6,7,8-tetrahydro-naphthalen-1-yloxy)-2,5-dihydro-pyrrol-1-yl]-pentanoic acid methyl ester
Ausbeute 15.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)O)N1CC(Oc2cccc3c2CCCC3)=CC1=O
Reaction #47340
(S)-4-methyl-2-[2-oxo-4-(5,6,7,8-tetrahydro-naphthalen-1-yloxy)-2,5-dihydro-pyrrol-1-yl]-pentanoic acid
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H]2COC(C)(C)O2)n1)N1CC(Oc2cccc3c2CCCC3)=CC1=O
Reaction #47341
(S)-4-methyl-2-[2-oxo-4-(5,6,7,8-tetrahydro-naphthalen-1-yloxy)-2,5-dihydro-pyrrol-1-yl]-pentanoic acid [1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl-methyl)-1H-pyrazol-3-yl]-amide
Ausbeute 48.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(C)c2C)=CC1=O
Reaction #47530
(S)-3-cyclohexyl-2-[4-(2,3-dimethyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
Ausbeute 30.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(OC2=CC(=O)N([C@@H](CC3CCCCC3)C(=O)O)C2)c1C
Reaction #47531
(S)-3-cyclohexyl-2-[4-(2,3-dimethyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(OC2=CC(=O)N([C@@H](CC3CCCCC3)C(=O)Nc3ccn(CC(C)(C)O)n3)C2)c1C
Reaction #47532
(S)-3-cyclohexyl-2-[4-(2,3-dimethyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1cnccn1)N1CC(Oc2cccc(CC(C)(C)O)c2)=CC1=O
Reaction #47681
(S)-2-{4-[3-(2-hydroxy-2-methyl-propyl)-phenoxy]-2-oxo-2,5-dihydro-pyrrol-1-yl}-4-methyl-pentanoic acid pyrazin-2-ylamide
Ausbeute 22.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49599
4-chloro-5-[3-(tert-butoxycarbonylamino)propoxy]-7-iodoisoindolinone
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCCOc1cc(I)c2c(c1Cl)CNC2=O
Reaction #49601
4-chloro-5-(3-aminopropoxy)-7-iodoisoindolinone hydrochloride
Ausbeute 193.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)cc(OC)c(C)c1C
Reaction #56128
9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid ethyl amide
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)cc(OC)c(C)c1C
Reaction #56135
9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid propargyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)cc(OC)c(C)c1C
Reaction #56147
9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid methyl amide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c(C=CC(C)=CC=CC(C)=CC(=O)NC(C)C)c(C)c1C
Reaction #56148
9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid isopropyl amide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)cc(OC)c(C)c1C
Reaction #56149
9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid butyl amide
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCNC(=O)C=C(C)C=CC=C(C)C=Cc1c(C)cc(OC)c(C)c1C
Reaction #56150
9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-oic acid hexylamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCc1c(OC)cccc1C(=O)NN(C(=O)c1cc(C)cc(C)c1)C(C)(C)C
Reaction #67913
3,5-dimethyl-benzoic acid N′-(2-allyloxymethyl-3-methoxy-benzoyl)-N-tert-butyl-hydrazide
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCOc1cc(-c2coc(C)c2C(N)=O)ccc1Cl
Reaction #78294
4-chloro-3-(3-methyl-2-butenyloxy)phenyl-2-methyl-3-furancarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NN)ccc1-n1cnc(C)c1.Cl.Cl
Reaction #158322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NN)ccc1-n1cnc(C)c1
Reaction #158323
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2ccc(F)c(F)c2)CCCn2c(-c3ccc(-n4cnc(C)c4)c(OC)c3)nnc21
Reaction #158325
title compound
Ausbeute 45.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter