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527942

CS(=O)(=O)O[C@H]1CCNC1=O
Reaction #62798
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC(Cc1ccccc1)C(=O)Nc1ccc(Br)cc1
Reaction #228346
DOI: 10.1039/C8SC04228D
CCC(OS(C)(=O)=O)C(N)=O
Reaction #389731
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCNC(CC)C(N)=O
Reaction #393953
DOI: 10.1039/C8SC04228D
CN1CCCC(OS(C)(=O)=O)C1=O
Reaction #401226
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OC1CCN(CC#CCN2CCCC2)C1=O
Reaction #406727
DOI: 10.1039/C8SC04228D
COc1cc(OC)c(CNC(=O)C(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)OS(=O)(=O)c2ccc(C)cc2)c(OC)c1
Reaction #490270
solid 11
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(CNC(=O)[C@@H](C[C@H](NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)OS(=O)(=O)c2ccc(C)cc2)c(OC)c1
Reaction #490271
(2S,4R)-tert-butyl-2-(tert-butoxycarbonylamino)-5-oxo-4-(tosyloxy)-5-(2,4,6-tri methoxybenzylamino)pentanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(CNC(=O)[C@H](C[C@H](NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)OS(=O)(=O)c2ccc(C)cc2)c(OC)c1
Reaction #490272
(2S,4S)-tert-butyl-2-(tert-butoxycarbonylamino)-5-oxo-4-(tosyloxy)-5-(2,4,6-tri methoxybenzylamino)pentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N2CC[C@@H](OS(C)(=O)=O)C2=O)CC1
Reaction #495056
(R)-tert-butyl 4-(3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N2CC[C@H](Oc3ccc(Br)cc3F)C2=O)CC1
Reaction #495061
(S)-tert-butyl 4-(3-(4-bromo-2-fluorophenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N2C[C@H](OCc3ccccc3)[C@@H](OS(C)(=O)=O)C2=O)CC1
Reaction #495094
tert-butyl 4-((3R,4S)-4-(benzyloxy)-3-(methylsulfonyloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N2C[C@H](OCc3ccccc3)[C@H](Oc3ccc(Br)cc3F)C2=O)CC1
Reaction #495095
tert-butyl 4-((3S,4S)-4-(benzyloxy)-3-(4-bromo-2-fluorophenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 40.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnnn1-c1ccc(OC2CCN(C3CCN(C(=O)OC(C)(C)C)CC3)C2=O)cc1
Reaction #495132
tert-butyl-4-(3-(4-(5-methyl-1H-tetrazol-1-yl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(O[C@H]2CCN(C3CCN(C(=O)OC(C)(C)C)CC3)C2=O)c(F)c1
Reaction #495135
(S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(N2CC[C@H](Oc3ccc4[nH]ncc4c3)C2=O)CC1
Reaction #495148
(S)-tert-butyl 4-(3-(1H-indazol-5-yloxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(O[C@H]2CCN(C3CCN(C(=O)OC(C)(C)C)CC3)C2=O)cn1
Reaction #495172
(S)-methyl 5-(1-(1-(tert-butoxycarbonyl)piperidin-4-yl)-2-oxopyrrolidin-3-yloxy)picolinate
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(O[C@H]2CCN(C3CCN(C(=O)OC(C)(C)C)CC3)C2=O)c(F)c1
Reaction #495181
(S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate
Ausbeute 83.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1[C@@H](OS(=O)(=O)c2ccc(C(F)(F)F)cc2)CCN1c1ccc(C(F)(F)F)cc1
Reaction #602061
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](C#N)C[C@H]1COc1cccnc1
Reaction #704540
title compound
Ausbeute 35.1%DOI: 10.6084/m9.figshare.5104873.v1
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