ferrocene

[Cl-].[Cl-].[Zr+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #6335
zirconocene dichloride
Ausbeute 118.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[C-]1=CC=CC1.[C-]1=CC=CC1.[Cl-].[Cl-].[Hf+4]
Reaction #6336
hafnocene dichloride
Ausbeute 137.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cc(C)cc(C)c1
Reaction #6337
mesitylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #304729
Ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
—
Reaction #319291
tetrachloroferrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
Nc1ncc(Br)nc1C(F)(F)F
Reaction #331766
title compound
Ausbeute 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C(CCCCl)[c-]1cccc1.[Fe+2].c1cc[cH-]c1
Reaction #336751
4-chlorobutyroylferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
O=C(CCCl)[c-]1cccc1.[Fe+2].c1cc[cH-]c1
Reaction #346470
chloropropionyl ferrocene
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
O=C(C1=C([c-]2cccc2)CCC1)c1ccccc1.[Fe+2].c1cc[cH-]c1
Reaction #346762
1-benzoyl-2-ferrocenylcyclopentene
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
O=C(CCCCC(=O)[c-]1cccc1)c1ccc(Cl)cc1.[Fe+2].c1cc[cH-]c1
Reaction #346765
5-(4-chlorobenzoyl)pentanoyl ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1.c1ccccc1
Reaction #461919
benzene ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
Cc1ccccc1.[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #461920
toluene ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
c1ccc2c(c1)CCCC2
Reaction #461921
Tetralin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
Cc1ccccc1.[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #461922
toluene ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
CC(C)(C)c1cc(C(C)(C)C)c2op(-[c-]3cccc3)oc3c(C(C)(C)C)cc(C(C)(C)C)cc3c2c1.CC(C)(C)c1cc(C(C)(C)C)c2op(-[c-]3cccc3)oc3c(C(C)(C)C)cc(C(C)(C)C)cc3c2c1.[Fe+2]
Reaction #486528
light brown solid
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CC(C)(C)c1cc2c(c(C(C)(C)C)c1)OP([c-]1cccc1)Oc1c(cc(C(C)(C)C)cc1C(C)(C)C)C2.CC(C)(C)c1cc2c(c(C(C)(C)C)c1)OP([c-]1cccc1)Oc1c(cc(C(C)(C)C)cc1C(C)(C)C)C2.[Fe+2]
Reaction #486529
light brown solid
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #495234
Ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #521023
desired compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
[C].[Fe+2].c1cc[cH-]c1.c1cc[cH-]c1
Reaction #531842
ferrocene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(O)c1cc2ccc(Cl)cc2c2cc(Br)ccc12
Reaction #636665
6-bromo-3-chlorophenanthrene-9-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
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