Teilstruktursuche

1267423

Cc1ccc2c(N3CCN(C(=O)OC(C)(C)C)CC3)cccc2n1
Reaction #44046
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCNCC3)cc(Cl)cc2n1
Reaction #44059
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(C(=O)OC(C)(C)C)CC3)cccc2n1
Reaction #44098
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN[C@H](C)C3)cccc2n1
Reaction #44130
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN[C@@H](C)C3)cccc2n1
Reaction #44134
title compound
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1c(O)c2cccnc2c2ncccc12
Reaction #47179
5,6-dihydroxy-1,10-phenanthroline
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c3c(ccc2n1)OC[C@@H](CO)O3
Reaction #56749
alcohol
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c3c(ccc2n1)OC[C@H](COS(=O)(=O)c1ccc(Br)cc1)O3
Reaction #56750
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c3c(ccc2n1)OCC(CN1CC(Cc2cn(C)c4ccc(F)cc24)C1)O3
Reaction #56760
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(-c3cccc(F)c3)cc(=O)c2c1OP(=O)(O)O
Reaction #66913
52
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2c1ccc(=O)n2CC=O
Reaction #68104
(5-methoxy-2-oxoquinolin-1(2H)-yl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=CCn1c(=O)ccc2c(OCc3ccccc3)cccc21
Reaction #68172
(5-benzyloxy-2-oxoquinolin-1(2H)-yl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2cccc(OC)c2c1=O
Reaction #161073
5-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2[nH]cc(C(=O)O)c(=O)c12
Reaction #161074
5-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c[nH]c2cccc(O)c2c1=O
Reaction #161083
5-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c[nH]c2cccc(O)c2c1=O
Reaction #161084
5-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
Ausbeute 87.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(Cc2ccccc2)c2c3c(nc4cccc(c24)O1)CCCC3
Reaction #195636
DOI: 10.1039/C8SC04228D
O=c1cc[nH]c2ccc3c(c12)OCCO3
Reaction #207653
DOI: 10.1039/C8SC04228D
COc1cc(NC(C)CCCN2C(=O)c3ccccc3C2=O)c2nccc(C)c2c1OCCCCCCCCCc1ccccc1
Reaction #222434
DOI: 10.1039/C8SC04228D
COC(=O)COc1ccc(Cl)c2nc(C)c(Oc3ccc(Cl)cc3)c(C)c12
Reaction #230809
DOI: 10.1039/C8SC04228D
Seite 1Weiter