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966950

O=C(COc1ccccc1)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)OCc1ccccc1
Reaction #1807655
(2S)-1-(N-benzyloxycarbonyl-L-prolyl)-2-(phenoxyacetyl)-pyrrolidine
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)OCc2ccccc2)cc1
Reaction #1807675
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)OCc2ccccc2)cc1
Reaction #1807676
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CCc1ccccc1
Reaction #1807677
title compound
Ausbeute 35.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)CCc2ccccc2)cc1
Reaction #1807678
title compound
Ausbeute 35.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)NCc1ccccc1
Reaction #1807679
title compound
Ausbeute 53.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)NCc2ccccc2)cc1
Reaction #1807680
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNC(=O)N2CCC[C@H]2C(=O)N2CCC[C@H]2C(O)COc2ccc(OC)cc2)cc1
Reaction #1807685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(Cl)cc1)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CCc1ccccc1
Reaction #1807689
title compound
Ausbeute 53.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCc1ccccc1)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(O)COc1ccc(OCc2ccccc2)cc1
Reaction #1807691
title compound
Ausbeute 81.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccc(O)cc1)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CCc1ccccc1
Reaction #1807692
title compound
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(O)COc1ccccc1
Reaction #1807699
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)cc1)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(O)COc1ccccc1
Reaction #1807700
title compound
Ausbeute 48.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(O)COc1ccccc1
Reaction #1807702
title compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(O)COc1ccccc1
Reaction #1807711
title compound
Ausbeute 82.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(O)COc1ccccc1
Reaction #1807712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)COc1ccccc1
Reaction #1807713
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)OC(C)(C)C)cc1
Reaction #1807714
title compound
Ausbeute 69.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)COc2ccccc2)cc1
Reaction #1807715
title compound
Ausbeute 149.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OCC(O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)CNc2ccccc2)cc1
Reaction #1807716
title compound
Ausbeute 95.9%DOI: 10.6084/m9.figshare.5104873.v1
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