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788886

CC(C)(C)OC(=O)N1CCCC1C(=O)N1CCN(Cc2ccccc2)CC1
Reaction #271323
DOI: 10.1039/C8SC04228D
CN1CCCC1CN1CCNCC1
Reaction #402809
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)N1CCN(C(=O)[C@@H]2C[C@H](NCc3cc(C(F)(F)F)cc(C(F)(F)F)c3)CN2Cc2ccccc2)CC1
Reaction #577818
title compound
Ausbeute 12.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CC(O)CN1)N1CCN(C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(Cc2ccccc2)C1
Reaction #1306803
DOI: 10.1039/C8SC04228D
CCCCCNC(=O)N1CC(=NOC)C[C@H]1C(=O)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1436216
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CC(=NOCc2ccc(Cl)c(Cl)c2)CN1C(=O)c1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1436228
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1ccc(C(=O)N2CC(=NOC(C)(C)C)C[C@H]2C(=O)N2CCN(Cc3ccc4c(c3)OCO4)CC2)c(=O)o1
Reaction #1436371
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C([C@@H]1C[C@@H](O)CN1)N1CCN(C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@H](Cc2ccccc2)C1
Reaction #1466400
(2R)-2-benzyl-1-[3,5-bis(trifluoromethyl)benzoyl]-4-[(4R)-4-hydroxy-L-prolyl]piperazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N1CCN(Cc2ccccc2)CC1
Reaction #1530229
desired product
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1CN1CCN(Cc2ccccc2)CC1
Reaction #1530230
desired product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1CN1CCNCC1
Reaction #1530231
desired product
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1615175
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCNC(=O)N1CC(=NOC)C[C@H]1C(=O)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1832215
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CC(=NOCc2ccc(Cl)c(Cl)c2)CN1C(=O)c1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1832224
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCc1ccc(C(=O)N2CC(=NOC(C)(C)C)C[C@H]2C(=O)N2CCN(Cc3ccc4c(c3)OCO4)CC2)c(=O)o1
Reaction #1832379
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCON=C1C[C@@H](C(=O)N2CCN(C(c3ccccc3)c3ccccc3)CC2)N(C(=O)COc2ccccc2)C1
Reaction #1832410
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)N1CCN(Cc2ccccc2)CC1
Reaction #2079895
desired product
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1CN1CCN(Cc2ccccc2)CC1
Reaction #2079896
desired product
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1CN1CCNCC1
Reaction #2079897
desired product
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.NCC(=O)N[C@@H]1CN[C@@H](C(=O)N2CCN(Cc3ccccc3)C[C@H]2CCc2ccccc2)C1
Reaction #2272657
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
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