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34959

CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCN(c2ccccc2)CC1
Reaction #5820
title compound
Выход 134.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCCN(C(=O)OCc2ccccc2)CC1
Reaction #5826
title compound
Выход 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CNC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)OC(C)(C)C
Reaction #5847
BOC-p-nitrophenylalanine 2-oxopropyl amide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(Oc2ccncc2)cc1)NC(=O)OC(C)(C)C
Reaction #41907
(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester
Выход 20.7%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
COC(=O)[C@H](Cc1ccc2nc(-c3c(Cl)cccc3Cl)ccc2c1)NC(=O)c1c(Cl)cncc1Cl
Reaction #43698
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1cc(F)cc(F)c1)NC(=O)OC(C)(C)C
Reaction #51489
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1cc(F)cc(F)c1)NC(=O)OC(C)(C)C
Reaction #51497
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1cc(F)cc(F)c1)NC(=O)OC(C)(C)C
Reaction #51498
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cc(F)cc(F)c1)C(=O)Cl
Reaction #51499
t-butyl-(1S)-2-chloro-1-[3,5-difluorobenzyl]-2-oxoethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O.NCC1(CC(=O)O)CCCCC1
Reaction #57044
Boc-Tyr Gabapentin
Выход 106.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(Oc2ccncc2)cc1)NC(=O)OC(C)(C)C
Reaction #67383
(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester
Выход 20.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc([N+](=O)[O-])cc1)C(=O)C=[N+]=[N-]
Reaction #88307
desired product
Выход 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(Cc1ccc([N+](=O)[O-])cc1)C(=O)C=[N+]=[N-]
Reaction #88329
desired product
Выход 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccc([N+](=O)[O-])cc1)C(=O)C=[N+]=[N-]
Reaction #88339
desired product
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)OC(C)(C)C
Reaction #91992
(S)-3-[4-nitrophenyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester
Выход 98.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)OC(C)(C)C
Reaction #91993
(S)-3-[4-aminophenyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester
Выход 100.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(c1cccc(OC2CCCCO2)c1)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #95971
racemic 2-(tert-butoxycarbonylamino)-3-(3'-tetrahydropyranyloxyphenyl)-3-butenoic acid
Выход 67.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@](Cc1ccccc1)(C(=O)O)C(C)(C)C
Reaction #162888
title compound
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cc1ccccc1)C(=O)O[C@H]1C[N+]2(CCOc3ccccc3)CCC1CC2.N[C@@H](Cc1ccccc1)C(=O)O[C@H]1C[N+]2(CCOc3ccccc3)CCC1CC2.O=C([O-])C(F)(F)F.O=C([O-])C(F)(F)F
Reaction #164213
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
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