piperidine DMF

—
Reaction #10028
hydroxamic acids
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCP(=O)(CC)C(CCCOc1ccc(C[C@H](N)C(=O)O)cc1)P(=O)(CC)CC
Reaction #67547
liquid 85
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CCP(=O)(CC=C)C(CCC(=O)NCCCC[C@H](N)C(=O)O)P(=O)(CC=C)CC=C
Reaction #67548
liquid 91
Ausbeute 85.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)CC(=O)N[C@@H](CCc1ccccc1S)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
Reaction #363297
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
C1CCNCC1.CN(C)C=O
Reaction #452858
piperidine DMF
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
—
Reaction #494139
amide-MBHA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Brc1nccs1.CCc1csc(Nc2ccc(Br)cc2)n1
Reaction #519617
bromothiazole N-(4-bromophenyl)-N-(4-ethyl-1,3-thiazol-2-yl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
CC(C)N=C=NC(C)C
Reaction #593947
DIPCDI
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC(C)C[C@@H](N)C(N)=O
Reaction #594477
D-Leu-NH2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
NC(=O)NCCC[C@H](NC(=O)CN1CN(c2ccccc2)C2(CCN(Cc3cccc4ccccc34)CC2)C1=O)C(N)=O
Reaction #738527
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
CNCCNC(=O)CCC(=O)O
Reaction #960738
N-(2-Methylamino-ethyl)-succinamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Brc1nccs1.CCc1csc(Nc2ccc(Br)cc2)n1
Reaction #984906
bromothiazole N-(4-bromophenyl)-N-(4-ethyl-1,3-thiazol-2-yl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_07
CC(C)C[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O
Reaction #1283913
Fmoc-Leu
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_05
O=C(N[C@@H](CSC(c1ccccc1)(c1ccccc1)c1ccccc1)C(=O)N1CCC[C@H]1C(=O)O)OCC1c2ccccc2-c2ccccc21
Reaction #1376515
Fmoc-Cys(Trt)-Pro
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
CC(C)(C)OC(=O)NCCCC[C@H](NCc1ccccc1)C(=O)O
Reaction #1484299
Benzyl Nε-(t-butoxycarbonyl)-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CC(C)C[C@@H](N)C(N)=O
Reaction #1681377
D-Leu-NH2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_11
CC(C)N=C=NC(C)C
Reaction #1704464
DIPCDI
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CC(C)C(=O)N(C1CCCCC1)[C@H]1CCN(NC(=O)[C@@H](Cc2ccc(Cl)cc2)NC2CN(C)C2)C1
Reaction #1757221
title compound
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
COC(=O)c1ccc2oc(-c3ccc(OC)cc3)cc2c1
Reaction #1881735
142
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
COC(=O)c1ccc2oc(-c3ccc(OC)cc3)cc2c1
Reaction #1923240
142
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_08
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