Teilstruktursuche

O=CCc1ccccc1

CCOC(=O)Cc1ccc(Br)cc1
Reaction #1303
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cccc(Br)c1
Reaction #1304
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(Br)cc1
Reaction #1458
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cccc(Br)c1
Reaction #1459
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc(O)cc1)OCc1ccccc1
Reaction #2320
benzyl 4-hydroxyphenylacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #3086
3-[((4-chloroanilino) carbonyl)methyl]phenol
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #3466
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-pentanone
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)Cc1cc(OC)ccc1NC(=O)OC(C)(C)C
Reaction #3477
1-(2-(tert-butoxycarbonylamino)-5-methoxyphenyl]-2-butanone
Ausbeute 74.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2cc(OC)ccc2[nH]1
Reaction #3478
2-ethyl-5-methoxy-1H-indole
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1cccc(O)c1)Nc1ccc(Cl)cc1
Reaction #6538
3-[((4-chloroanilino) carbonyl)methyl]phenol
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
Reaction #7753
desired product
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cc(Cl)ccc1O
Reaction #11747
(5-chloro-2-hydroxy-phenyl)-acetic acid
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1-c1cn[nH]c1
Reaction #40715
4-(2-fluorophenyl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2ccc3c(c2)nc(Cc2ccc(Br)cc2)n3C)ccn1
Reaction #41767
(4-{2-[(4-bromophenyl)methyl]-1-methylbenzimidazol-5-yloxy)-(2-pyridyl))-N-methylcarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(I)cc1
Reaction #42728
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cccc(-n2cccn2)c1
Reaction #44062
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCc1cccc(I)c1
Reaction #44170
title compound
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)Cc1ccccc1F)c1ccccc1
Reaction #46640
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cc1cccc(O)c1
Reaction #47650
3-(2-hydroxy-2-methyl-propyl)-phenol
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cccnc2NC1c1ccccc1
Reaction #49815
3(R,S)-Phenyl-3,4-dihydro-1,4,5-triazanaphthalen-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter