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443039

C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2009
N-(t-Butoxycarbonyl)-D-homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(C=O)Cc1ccc2ccccc2c1
Reaction #8631
aldehyde
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #40358
intermediate 1-6
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)O
Reaction #42318
(2S)-3-[4-(benzyloxy)phenyl]-2-[(tert-butoxycarbonyl)amino]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1ccccc1)C(=O)O
Reaction #56084
L-phenylalanine
Ausbeute 64.5%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](N)Cc1ccc(OCc2ccccc2)cc1
Reaction #64403
title compound
Ausbeute 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C=[N+]=[N-]
Reaction #64789
(S)-3-[[[(1,1-Dimethylethyl)oxy]carbonyl]amino]-2-oxo-1-diazo-4-phenylbutane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C=[N+]=[N-]
Reaction #64809
(S)-3-[[[(1,1-Dimethylethyl)oxy]carbonyl]amino]-2-oxo-1-diazo-4-phenylbutane
DOI: 10.6084/m9.figshare.5104873.v1
NCC(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)O
Reaction #67543
N-(N-(glycyl)-L-phenylalanyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #67544
gum
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #75988
tert-butyl (1R)-1-benzyl-2-oxopropylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #80481
compound 5
Ausbeute 8042.2%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #89574
[(S)-1-(methoxy-methyl-carbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester
Ausbeute 101.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #89578
title compound
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@H](Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #89579
benzyl (2S)-2-amino-3-phenyl-propanoate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCCCC[NH-].CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@H](C(=O)O)C(C)C
Reaction #93626
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(C)C
Reaction #93627
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(Cc1ccc(-c2ccccc2)cc1)NC(=O)OC(C)(C)C
Reaction #158066
tert-butyl 4-(biphenyl-4-yl)-3-(tert-butoxycarbonylamino)butanoate
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H](CO)C(=O)NCc1ccccc1
Reaction #161297
(R)-2-amino-N-benzyl-3-hydroxypropionamide
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(N)=S
Reaction #161908
#13
Ausbeute 130.6%DOI: 10.6084/m9.figshare.5104873.v1
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