Teilstruktursuche

C(C(=O)N)N.Cl

CC(C)C[C@H](NC(=O)CN)C(=O)N[C@@H](C)C(=O)OCc1ccccc1.Cl
Reaction #5080
H-Gly-Leu-Ala-OBzl HCl
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCCCC1)N1CC[C@H](NS(=O)(=O)/C=C/c2ccc(Cl)cc2)C1=O
Reaction #7395
title compound
Ausbeute 21.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)/C=C/c2ccc(Cl)c(O)c2)C1=O
Reaction #7419
title compound
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11674
title compound
Ausbeute 26.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11675
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11676
title compound
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccccc2N(CCO)C1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11678
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11679
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11680
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1Cc2ccccc2CNC1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11693
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@H]1Cc2ccccc2CNC1=O
Reaction #11696
(S)-4-amino-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccccc2CNC1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11697
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)OCc1ccccc1)NCc1nncn1-c1ccc(Cl)cc1C(=O)c1ccccc1
Reaction #54220
5-chloro-2-[3-(N-carbobenzoxyglycyl)aminomethyl-4H-1,2,4-triazol-4-yl]-benzophenone
Ausbeute 35.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59399
title compound
Ausbeute 26.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59401
title compound
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccccc2N(CCO)C1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #59403
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter