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926647

C#CC[C@H](NC(=O)CN1CCOCC1)C(=O)N[C@@H](Cc1ccc(OC)cc1)C(=O)OCc1ccccc1
Reaction #87074
(S)-Benzyl 3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)pent-4-ynamido)propanoate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)N)C(=O)OCc2ccccc2)cc1
Reaction #87081
(S)-benzyl 2-((S)-2-aminopropanamido)-3-(4-methoxyphenyl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)OCc2ccccc2)cc1
Reaction #87082
(S)-benzyl 3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoate
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)O)cc1
Reaction #87083
(S)-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoic acid
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)O)cc1
Reaction #87085
(2S,3R)-3-hydroxy-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoic acid
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](CO)NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #87087
(2S,3R)-benzyl 2-((S)-2-((tert-butoxycarbonyl)amino)-3-hydroxypropanamido)-3-hydroxy-3-(4-methoxyphenyl)propanoate
Ausbeute 93.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@@H](N)CO)C(=O)OCc2ccccc2)cc1
Reaction #87088
(2S,3R)-benzyl 2-((S)-2-amino-3-hydroxypropanamido)-3-hydroxy-3-(4-methoxyphenyl)propanoate
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](CO)NC(=O)CN2CCOCC2)C(=O)OCc2ccccc2)cc1
Reaction #87089
(2S,3R)-benzyl 3-hydroxy-2-((S)-3-hydroxy-2-(2-morpholinoacetamido)propanamido)-3-(4-methoxyphenyl)propanoate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](CO)NC(=O)CN2CCOCC2)C(=O)O)cc1
Reaction #87090
(2S,3R)-3-hydroxy-2-((S)-3-hydroxy-2-(2-morpholinoacetamido)propanamido)-3-(4-methoxyphenyl)propanoic acid
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)CN2CCC(O)CC2)C(=O)OCc2ccccc2)cc1
Reaction #87095
(S)-benzyl 2-((S)-2-(2-(4-hydroxypiperidin-1-yl)acetamido)propanamido)-3-(4-methoxyphenyl)propanoate
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CN1CCOCC1)C(=O)N[C@@H](Cc1ccc(OCc2ccccc2)c(OCc2ccccc2)c1)C(=O)O
Reaction #87179
(S)-3-(3,4-Bis(benzyloxy)phenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Cc1ccc(OCCCF)cc1)NC(=O)C1CCCCN1S(=O)(=O)c1cccc(F)c1
Reaction #245112
DOI: 10.1039/C8SC04228D
CC(C)Oc1ccc(CC(NC(=O)C2CCCCN2S(=O)(=O)c2cccc(F)c2)C(=O)O)cc1
Reaction #392165
DOI: 10.1039/C8SC04228D
—
Reaction #416735
Amino acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)[C@H](CC(=O)OCc1ccccc1)NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)OCc1ccccc1
Reaction #551734
30
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=N)NCCC[C@@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2ccc(OCc3ccccc3)cc2)C(=O)OCc2ccccc2)cc1
Reaction #554539
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=N)NCCC[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2ccc(OCc3ccccc3)cc2)C(=O)OCc2ccccc2)cc1
Reaction #554540
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=N)NCCC[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](COCc2ccccc2)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2ccc(OCc3ccccc3)cc2)C(=O)OCc2ccccc2)cc1
Reaction #554541
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=N)NCCC[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](COCc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2ccc(OCc3ccccc3)cc2)C(=O)OCc2ccccc2)cc1
Reaction #554542
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(C[C@H](NC(=O)[C@@H]2CCCCN2S(=O)(=O)c2cccc(F)c2)C(=O)OCc2ccccc2)cc1
Reaction #591331
title compound
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
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