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CCOCCl

O=C(OCc1ccccc1)N1CCCNCC1
Reaction #5825
title compound
Ausbeute 65.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1ccc(O)c(O)c1)OCc1ccccc1
Reaction #5999
desired compound
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1
COC1O[C@H]2[C@H](OCc3ccccc3)[C@@H]1N(C(=O)OCc1ccccc1)C[C@@H]2OCc1ccccc1
Reaction #6528
Methyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranoside
DOI: 10.6084/m9.figshare.5104873.v1
C=C1c2ccc(OC)cc2CCN1C(=O)OCc1ccccc1
Reaction #6858
6-methoxy-1-methylene-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC[C@@H](NC(=O)OCc1ccccc1)C(=O)OC
Reaction #7381
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1ccc(NC(=O)OCc2ccccc2)cc1F
Reaction #8249
title product
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(NC(=O)OCc3ccccc3)cc2F)cn1
Reaction #8253
title product
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=CC(=O)CCN1C(=O)OCc1ccccc1
Reaction #8621
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(NOC(=O)OCc2ccccc2)nc1C
Reaction #9188
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CC(C)CN1C(=O)OCc1ccccc1
Reaction #9989
(2S)-1-benzyloxycarbonyl-4-methylproline methyl ester
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CNC(=O)OCc2ccccc2)c1C(=O)OC
Reaction #10052
product
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(C(=O)O)cc1)OCc1ccccc1
Reaction #11958
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(COC(=O)NC(C)CC(=O)O)c([N+](=O)[O-])cc1OC
Reaction #40290
3-(4,5-dimethoxy-2-nitrobenzyloxycarbonylamino)-butyric acid
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)Nc1nc2c(s1)CN(C(=O)OCc1ccccc1)CC2
Reaction #40346
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CCOC1=O)OCc1ccccc1
Reaction #40697
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(CO)Cc1cccs1)OCc1ccccc1
Reaction #40711
title compound
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)C1CCN1C(=O)OCc1ccccc1
Reaction #40909
desired compound
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@](C)(Cc1ccc(O)cc1)NC(=O)OCc1ccccc1
Reaction #41859
(S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-2-methyl-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc2cc[nH]c12)OCc1ccccc1
Reaction #41976
title compound
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H]1OC(=O)[C@]1(CCCC)C(=O)OCc1ccccc1
Reaction #42001
β-lactone
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1
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