Teilstruktursuche

366133

C=C[C@@H]1C[C@]1(N)C(=O)OCC.Cl
Reaction #46071
ethyl 1(R)-amino-2(S)-vinylcyclopropane carboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)O
Reaction #46084
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)NS(=O)(=O)C1CC1
Reaction #46085
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OC(C)(C)C)c1ncc(-c2ccc(Br)cc2)[nH]1
Reaction #49161
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)OC
Reaction #51454
methyl 2(R/S)-(tert-butoxycarbonyl)amino-3,3-dimethyl4-pentenoate
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc([C@@H](N)C(C)C)n1
Reaction #52039
(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC(=O)OCc1ccccc1)C(=O)N[C@H](C(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](CCC(=O)OCc1ccccc1)C(=O)O)[C@@H](C)OCc1ccccc1
Reaction #54611
Boc-Val-Asp(OBzl)-Thr(Bzl)-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OH
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H](C(=O)N1CCC[C@H]1c1cccc(Oc2ccccc2)c1)C1CCCCC1
Reaction #57348
{(S)-1-Cyclohexyl-2-oxo-2-[(S)-2-(3-phenoxy-phenyl)-pyrrolidin-1-yl]-ethyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(C(=O)N1CCC[C@H]1c1nnn(Cc2ccccc2)n1)C1CCCCC1
Reaction #57353
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C(=NOCc2ccccc2)CCN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C1CCCCC1
Reaction #57358
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(N)C(=O)OC.Cl
Reaction #61359
compound 20b
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)cc1
Reaction #64239
N-(t-butoxycarbonyl)-L-valine 4-methoxy-1-phenylethylamide
Ausbeute 217.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](C)NC[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #72423
desired compound
Ausbeute 43.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)C(=O)O
Reaction #72424
desired compound ( 20 )
Ausbeute 191.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75559
solid
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCC[C@@H](COC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)Cn1cnc2c(=O)[nH]c(N)nc21
Reaction #76837
pure title compound
Ausbeute 39.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](N)C(=O)OC1CCC(n2cc(-c3ccc(Oc4ccccc4)cc3)c3c(N)ncnc32)C1.Cl
Reaction #79792
3-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclopentyl (2S)-2-amino-3-methylbutanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)OC(O)C(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #81343
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methylbutyric acid [11β,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](N)C(=O)OC(O)C(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C.O=C(O)C(F)(F)F
Reaction #81344
(2S)-2-amino-3-methyl-butyric acid [11β,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester trifluoroacetate
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)OC(O)C(=O)[C@H]1[C@H](C)C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #81345
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methyl-butyric acid [11β,21-dihydroxy-6α-fluoro-16α-methyl-3,20-dioxo-pregna-1,4-dien-21-yl] ester
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
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