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527047

CC[C@H](NC(=O)C(CC)(CC)NC(=O)[C@@H](N)CC(=O)O)c1ccccc1
Reaction #867
α-L-aspartyl-α,α-diethylglycine (S)-α-ethylbenzylamide
Выход 29.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCNC1=O
Reaction #2840
title compound
Выход 85.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CO)[C@H](NC1(c2ccccc2)c2ccccc2-c2ccccc21)C(=O)OCc1ccccc1
Reaction #46648
(2S,3S)-benzyl 4-hydroxy-3-methyl-2-(9-phenyl-9H-fluoren-9-ylamino)butanoate
Выход 34.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CO)[C@H](NC1(c2ccccc2)c2ccccc2-c2ccccc21)C(=O)OCc1ccccc1
Reaction #49138
(2S,3S)-benzyl 4-hydroxy-3-methyl-2-(9-phenyl-9H-fluoren-9-ylamino)butanoate
Выход 34.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(C(=O)OC)(C(C)(C)NC(=O)OCc1ccccc1)S(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #51456
methyl 2(R/S)-[4-(4-fluorophenoxy)benzenesulfonyl][(ethoxycarbonyl)methyl]amino-3-(benzyloxycarbonyl)amino-3-methylbutanoate
Выход 75.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1[C@H](NC(C)=O)C(=O)O[C@@H]1C
Reaction #83736
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1[C@H](C)OC(=O)[C@@H]1NC(C)=O
Reaction #83737
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1OC(=O)[C@@H](N)[C@@H]1C(=O)O
Reaction #83738
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1[C@H](N)C(=O)O[C@@H]1C.Cl
Reaction #83739
2(S)-amino-3(S)-methoxycarbonyl-4(R)-pentanolide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@@H](C(=O)O)[C@H](N)C(=O)O
Reaction #83740
2(S)-amino-3(S)-carboxy-4(R)-hydroxypentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]([C@H](N)C(=O)O)[C@@H](C)O
Reaction #83741
2(S)-amino-3(S)-ethoxycarbonyl-4(R)-hydroxy-pentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C2CC=CCN2C(=O)C2CCNCC2C(=O)OC(C)(C)C)c1
Reaction #89703
4-(3-Isopropyl-phenyl-3,6-dihydro-2H-pyridine-1-carbonyl]-piperidine-3-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@H]1CC(=O)CN(C(=O)OCc2ccccc2)[C@@H]1C(=O)OCc1ccccc1
Reaction #89704
ketone
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C1C[C@H](C(=O)OC(C)(C)C)[C@@H](C(=O)OCc2ccccc2)N(C(=O)OCc2ccccc2)C1
Reaction #89705
1,2-dibenzyl 3-tert-butyl(2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylate
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CN[C@H](C(=O)O)[C@@H](C(=O)OC(C)(C)C)C1
Reaction #89706
(2S,3S)-3-(tert-butoxycarbonyl)-5-(2-methoxy-2-oxoethyl)piperidine-2-carboxylic acid
Выход 88.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CN[C@H](C(=O)N2CCC(c3ccccc3)C2)[C@@H](C(=O)OC(C)(C)C)C1
Reaction #89707
crude product
Выход 104.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)O[C@@H]1C[C@H](C(=O)OC)[C@@H](C(=O)OCc2ccccc2)N(Cc2ccccc2)C1
Reaction #89717
product
Выход 69.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](O)CN(Cc2ccccc2)[C@@H]1C(=O)OCc1ccccc1
Reaction #89718
alcohol
Выход 100.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](O)CN[C@@H]1C(=O)O
Reaction #89719
(2S,3S,5R)-5-hydroxy-3-(methoxycarbonyl)piperidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](O)CN(C(=O)OC)[C@@H]1C(=O)N1CCN(c2ccccc2)CC1
Reaction #89720
titled compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
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