Teilstruktursuche

945208

O=C(CBr)c1ccc(OCCCCl)cc1F
Reaction #8460
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3F)nc2c1
Reaction #8461
2-(4′-chloropropoxy-2′fluorophenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(OCCCCl)cc1F
Reaction #1159210
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3F)nc2c1
Reaction #1159211
2-(4′-chloropropoxy-2′fluorophenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3F)nc2c1
Reaction #1355858
2-(4′-chloropropoxy-2′fluorophenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(-c2csc(N)n2)c(Cl)c1
Reaction #1552728
4-(2-chloro-6-fluoro-4-methoxyphenyl)thiazol-2-ylamine
Ausbeute 42.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Oc2cc(C)c(-c3csc(N)n3)c(F)c2)cc1
Reaction #1552765
4-(2-fluoro-4-(4-methoxyphenoxy)-6-methylphenyl)thiazol-2-ylamine
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2csc(-c3ccc(-c4ccccc4[N+](=O)[O-])c(C(=O)O)c3)n2)c(F)c1
Reaction #1606467
4-[4-(2-Fluoro-4-methoxy-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(OCCCCl)cc1F
Reaction #1911679
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3F)nc2c1
Reaction #1911680
2-(4′-chloropropoxy-2′fluorophenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(OCCCCl)cc1F
Reaction #1911713
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3F)nc2c1
Reaction #1911714
2-(4′-chloropropoxy-2′fluorophenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(C(=O)CBr)cc1C#N
Reaction #2263026
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c([C@H]2CN3CCN(C(=O)OC(C)(C)C)C[C@@H]3CO2)cc1C#N
Reaction #2263027
desired product
DOI: 10.6084/m9.figshare.5104873.v1