Substructure Search

774092

CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)C(Cl)Cl
Reaction #193091
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)C(Cl)Cl
Reaction #261208
DOI: 10.1039/C8SC04228D
C[C@H](NC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)CCl
Reaction #323645
Z-Phe-Gly-Ala-TyrCH2Cl
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #501169
(S)-3-amino-1-chloro-4-phenyl-2-butanone hydrochloride
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)CCl)OCc1ccccc1
Reaction #501171
(3S)-3-benzyloxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #501172
(3S)-3-methoxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)CCl
Reaction #1067591
Z-Phe-Gly-Ala-TyrCH2Cl
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C(Cl)Cl
Reaction #1076635
(3S)-3-tert-butoxycarbonylamino-1,1-dichloro-4-phenyl-2-butanone
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C(Cl)Cl
Reaction #1076636
(3S)-3-tert-butoxycarbonylamino-1,1-dichloro-4-phenyl-2-butanone
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(Cl)Cl)[C@H](Cc1ccccc1)N=C(c1ccccc1)c1ccccc1
Reaction #1076638
(3S)-1,1-dichloro-3-(diphenylmethylene) amino-4-phenyl-2-butanone
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(Cl)Cl)[C@H](Cc1ccccc1)N(Cc1ccccc1)Cc1ccccc1
Reaction #1076640
(3S)-1,1-dichloro-3-dibenzylamino-4-phenyl-2-butanone
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)C(Cl)C(=O)C(Cl)C(=O)[C@H](Cc1ccccc1)NC(=O)C1CCCCC1)C1CCCCC1
Reaction #1153237
titled compound
Yield 162.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1159059
(S)-3-amino-1-chloro-4-phenyl-2-butanone hydrochloride
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)CCl)OCc1ccccc1
Reaction #1159061
(3S)-3-benzyloxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1159062
(3S)-3-methoxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)C(Cl)C(=O)C(Cl)C(=O)[C@H](Cc1ccccc1)NC(=O)C1CCCCC1)C1CCCCC1
Reaction #1193815
titled compound
Yield 162.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C(Cl)Cl
Reaction #1455909
tert-butyl (S)-(1-benzyl-3,3-dichloro-2-oxopropyl)carbamate
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)CCl
Reaction #1467793
Z-Phe-Gly-Ala-TyrCH2Cl
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)C(Cl)Cl
Reaction #1650218
DOI: 10.1039/C8SC04228D
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1928836
(3S)-3-methoxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
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