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624996

C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N)C1=O
Reaction #7387
title compound
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)c2cc3cc(Cl)ccc3o2)C1=O
Reaction #7416
title compound
Ausbeute 55.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C#N)cc(C(=O)O)c1
Reaction #42274
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(N)=O)cc(C(=O)O)c1
Reaction #42275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC)cc(C(=O)OC)c1
Reaction #42280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC)cc(C(=O)O)c1
Reaction #42281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(CC#N)cc(C(=O)O)c1
Reaction #42302
3-(cyanomethyl)-5-[(dipropylamino)carbonyl]benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cc(C(=O)OC)cc(C(=O)N(CCC)CCC)c1
Reaction #42305
methyl 3-[(dipropylamino)carbonyl]-5-ethynylbenzoate
Ausbeute 111.3%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cc(C(=O)O)cc(C(=O)N(CCC)CCC)c1
Reaction #42306
3-[(dipropylamino)carbonyl]-5-ethynylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncc[nH]2)c1
Reaction #42340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42349
methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2nccn2COCC)c1
Reaction #42351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2nccs2)c1
Reaction #42566
methyl 3-[(dipropylamino)carbonyl]-5-(1,3-thiazol-2-yl)benzoate
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42570
methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoate
Ausbeute 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42571
methyl 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoate
Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42579
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42580
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C#N)cc(C(=O)OC)c1
Reaction #42617
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CN1CCN(Cc2ccccc2)C1=O
Reaction #51837
tert-butyl 2-(2-oxo-3-benzylimidazolidinyl)acetate
Ausbeute 87.9%DOI: 10.6084/m9.figshare.5104873.v1
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