Teilstruktursuche

3712

CCOC(=O)C(=CN(c1cc(N2CCNCC2)c(F)c(C)c1[N+](=O)[O-])C1CC1)C(=O)OCC
Reaction #1387
diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(SC)nc1O
Reaction #7509
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8564
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8565
title compound
Ausbeute 78.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8566
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8567
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8568
title compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8569
title compound
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8570
title compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8571
title compound
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8572
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8573
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8574
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8575
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8576
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8580
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CNc1cc(N)nc(SC)n1)C(=O)OCC
Reaction #44526
diethyl 2-(((6-amino-2-(methylsulfanyl)-4-pyrimidinyl)amino)methylene)malonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CNc1cscc1C)C(=O)OCC
Reaction #51892
solid
DOI: 10.6084/m9.figshare.5104873.v1
Br.Fc1ccc2nccc(OCCCBr)c2c1
Reaction #69081
titled compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter