Teilstruktursuche

1253

COC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)OCc1ccccc1
Reaction #3154
N-Benzyloxycarbonyl-O-methyl-tyrosine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCN(c2ccccc2)CC1
Reaction #5820
title compound
Ausbeute 134.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCCN(C(=O)OCc2ccccc2)CC1
Reaction #5826
title compound
Ausbeute 97.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CC2CC(C1)c1cc([N+](=O)[O-])c(O)cc12)C(F)(F)F
Reaction #10191
oil
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2c(cc1O)C1CC2CN(C(=O)C(F)(F)F)C1
Reaction #10192
2,2,2-Trifluoro-1-(4-hydroxy-5-amino-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1ccc2c(c1)OCCO2
Reaction #41299
(S)-tert-butyl 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-oxopropan-2-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)O
Reaction #42318
(2S)-3-[4-(benzyloxy)phenyl]-2-[(tert-butoxycarbonyl)amino]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43063
3-{2-[2-(4-Hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(Cc2cccc(-c3ccnc(NCCc4ccc(O)cc4)n3)c2)CC1
Reaction #43064
4-(2-{4-[3-(4-Methyl-piperazin-1-ylmethyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(CCNc2nccc(-c3cccc(CNc4cnccn4)c3)n2)cc1
Reaction #43115
4-(2-{4-[3-(Pyrazin-2-ylaminomethyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CCNCc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43122
4-{2-[4-(3-Ethylaminomethyl-phenyl)-pyrimidin-2-ylamino]-ethyl}-phenol
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C(=S)NN)OCO3
Reaction #53336
crude product
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C#N)OCO3
Reaction #53337
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C(N)=NO)OCO3
Reaction #53338
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NNC(=S)N1N=C(c2ccc([N+](=O)[O-])cc2)c2cc3c(cc2C[C@H]1C)OCO3
Reaction #53352
(R)—N′-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbothioyl}-acetic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nnn[nH]1)OCO3
Reaction #53360
title compound
Ausbeute 101.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](Cc1cc(I)c(Oc2cc(I)c(O)c(I)c2)c(I)c1)NC(=O)C(F)(F)F
Reaction #56344
thyroxine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O.NCC1(CC(=O)O)CCCCC1
Reaction #57044
Boc-Tyr Gabapentin
Ausbeute 106.7%DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(C(O)CNC2(Cc3ccccc3)CC2)ccc1O
Reaction #58126
4-[2-(1-benzyl-cyclopropylamino)-1-hydroxy-ethyl]-2-hydroxymethyl-phenol
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter