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CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](OC(=O)c3ccc([N+](=O)[O-])cc3)C[C@@H]2C1
Reaction #659221
tert-butyl (8S,9aR)-8-[(4-nitrobenzoyl)oxy]-5-oxohexahydro-1H-pyrrolo[1,2-a][1,4]diazepine-2(3H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](O)C[C@@H]2C1
Reaction #659222
titled compound
Ausbeute 64.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #659223
titled compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #659225
titled compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659226
(8R,9aR)-8-[(5-cyclopropylpyrazin-2-yl)oxy]octahydro-5H-pyrrolo[1,2-a][1,4]diazepin-5-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](O)C[C@H]2C1
Reaction #659230
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](Oc3cnc(C4CC4)cn3)C[C@H]2C1
Reaction #659231
title compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #659232
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](OC(=O)c3ccc([N+](=O)[O-])cc3)C[C@@H]2C1
Reaction #1137489
tert-butyl (8S,9aR)-8-[(4-nitrobenzoyl)oxy]-5-oxohexahydro-1H-pyrrolo[1,2-a][1,4]diazepine-2(3H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](O)C[C@@H]2C1
Reaction #1137490
titled compound
Ausbeute 64.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #1137491
titled compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@H](Oc3cnc(C4CC4)cn3)C[C@@H]2C1
Reaction #1137493
titled compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@H]2C[C@@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #1137494
(8R,9aR)-8-[(5-cyclopropylpyrazin-2-yl)oxy]octahydro-5H-pyrrolo[1,2-a][1,4]diazepin-5-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](O)C[C@H]2C1
Reaction #1137499
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)N2C[C@@H](Oc3cnc(C4CC4)cn3)C[C@H]2C1
Reaction #1137500
title compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCNC[C@@H]2C[C@H](Oc3cnc(C4CC4)cn3)CN12
Reaction #1137501
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cncc(N2C3CCNCC2CC3)c1.O=C(O)/C=C/C(=O)O
Reaction #1354156
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cncc(N2C3CCC2CN(C(=O)OC(C)(C)C)CC3)c1
Reaction #1354157
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2CCC(C1)N2
Reaction #1354158
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2CCC(C1)N2c1ccc(Cl)nc1
Reaction #1635215
DOI: 10.1039/C8SC04228D
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