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419283

Cc1cc(C2(O)CC3CN(C(=O)OC(C)(C)C)CC3C2)cnc1Cl
Reaction #236270
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CC(O)CC2C1
Reaction #290065
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #331727
1,1-dimethylethyl (3aR,6aS)-5-(hydroxy)-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(=O)CC2C1
Reaction #406341
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #532688
1,1-dimethylethyl (3aR,6aS)-5-(hydroxy)-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #533896
(3aR,6aS)-tert-butyl 5-hydroxyhexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #543040
1,1-dimethylethyl (3aR,6aS)-5-(hydroxy)-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #650208
1,1-dimethylethyl (3aR,6aS)-5-(hydroxy)-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(O)CC2C1
Reaction #781985
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #792845
1,1-dimethylethyl (3aR,6aS)-5-(hydroxy)-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(O)CC2C1
Reaction #907059
DOI: 10.1039/C8SC04228D
CC1C(=O)CC2CN(C(=O)OC(C)(C)C)CC21
Reaction #964872
tert-butyl 4-methyl-5-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C(NCc2ccccc2)CC2CN(C(=O)OC(C)(C)C)CC21
Reaction #964873
tert-butyl 5-(benzylamino)-4-methylhexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CC(O)C[C@H]2C1
Reaction #1098507
1,1-dimethylethyl (3aR,6aS)-5-(hydroxy)-hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(=O)CC2C1
Reaction #1143812
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(NCc3ccccc3)CC2C1
Reaction #1143813
title compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(O)CC2C1
Reaction #1146533
title compound
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cncc(C2(O)CC3CN(C(=O)OC(C)(C)C)CC3C2)c1
Reaction #1303410
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CC(=O)CC2C1
Reaction #1565164
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CC(NCc3ccccc3)CC2C1
Reaction #1565165
title compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1
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