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O=C(O)CCI

COC(=O)C1(CI)CCCC1
Reaction #44866
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CN2CCC(CNC(=O)OC(C)(C)C)CC2)CCCC1
Reaction #44867
title compound
Ausbeute 67.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CN2CCC(O)(CNC(=O)OC(C)(C)C)CC2)CCCCC1
Reaction #44875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1(F)CCN(CC2(C(=O)OCc3ccccc3)CCOCC2)CC1
Reaction #44888
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(C(F)(F)F)cc1)C(=O)OC(C)(C)C
Reaction #48300
(S)-methyl 2-(tert-butoxycarbonyl)-3-(4-(trifluoromethyl)phenyl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1nc(Cl)cs1)C(=O)OC(C)(C)C
Reaction #48308
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1cnc([Si](C(C)C)(C(C)C)C(C)C)s1)C(=O)OC(C)(C)C
Reaction #48309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC(O)c1ccc(OC)c(I)n1
Reaction #83556
(5RS)-5-hydroxy-5-(2-iodo-3-methoxy-6-pyridyl)-pentanoic acid methyl ester
Ausbeute 72.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccnc(OC)c1)NC(=O)OC(C)(C)C
Reaction #87075
(S)-methyl 2-(tert-butoxycarbonylamino)-3-(2-methoxypyridin-4-yl)propanoate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1=CC(=O)CC1)NC(=O)OC(C)(C)C
Reaction #87109
(S)-methyl 2-(tert-butoxycarbonylamino)-3-(3-oxocyclopent-1-enyl)propanoate
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CI)NC(=O)OC(C)(C)C
Reaction #87114
(R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1=CCCC1)NC(=O)OC(C)(C)C
Reaction #87115
(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(cyclopent-1-en-1-yl)propanoate
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1=CCCC1)NC(=O)OC(C)(C)C
Reaction #87121
(S)-Methyl 2-(tert-butoxycarbonylamino)-3-cyclopentenylpropanoate
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CI)NC(=O)OCc1ccccc1
Reaction #87130
(R)-methyl 2-(benzyloxycarbonylamino)-3-iodopropanoate
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc2[nH]ccc2c1)NC(=O)OCc1ccccc1
Reaction #87131
(S)-methyl 2-(benzyloxycarbonylamino)-3-(1H-indol-5-yl)propanoate
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(C)c(OCc2ccccc2)c1)NC(=O)OC(C)(C)C
Reaction #87133
(S)-methyl 3-(3-(benzyloxy)-4-methylphenyl)-2-((tert-butoxycarbonyl)amino)propanoate
Ausbeute 37.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1ccc2c(c1)CCN(Cc1ccc(OC)cc1OC)S2(=O)=O)NC(=O)OC(C)(C)C
Reaction #87140
(R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(2-(2,4-dimethoxybenzyl)-1,1-dioxido-3,4-dihydro-2H-benzo[e][1,2]thiazin-6-yl)propanoate
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccc(O)c(OCc2ccccc2)c1)C(=O)OCc1ccccc1)OCc1ccccc1
Reaction #90508
(S)-benzyl 3-(3-(benzyloxy)-4-hydroxyphenyl)-2-(((benzyloxy)carbonyl)amino)propanoate
Ausbeute 104.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(F)(F)Cc1ccc(OC)cc1
Reaction #175680
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccnc(C(F)(F)F)c1)C(=O)OC(C)(C)C
Reaction #183993
DOI: 10.1039/C8SC04228D
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