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1132160

CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS(C)(=O)=O)NC(=O)OCc1ccccc1)C(=O)[NH2+][O-].N#N.O
Reaction #82370
N2 [3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate
Выход 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS(C)(=O)=O)NC(=O)OCc1ccccc1)C(=O)[NH2+][O-].N#N.O
Reaction #354321
N2 [3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate
Выход 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS(C)(=O)=O)NC(=O)OCc1ccccc1)C(=O)[NH2+][O-].N#N.O
Reaction #554051
N2 [3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate
Выход 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS(C)(=O)=O)NC(=O)OCc1ccccc1)C(=O)[NH2+][O-].N#N.O
Reaction #830060
N2 [3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate
Выход 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS(C)(=O)=O)NC(=O)OCc1ccccc1)C(=O)[NH2+][O-].N#N.O
Reaction #1844934
N2 [3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate
Выход 34.5%DOI: 10.6084/m9.figshare.5104873.v1