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293140

CC1=C(C)C(c2ccccc2C(O)c2ccccc2)C(C)=C1C
Reaction #43976
{2-(2,3,4,5-tetramethylcyclopentadienyl)phenyl}phenylmethylalcohol
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(c2ccccc2CNc2cc(C)cc(C)c2)C(C)=C1C
Reaction #43983
N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(c2ccccc2CNc2cc(C)cc(C)c2)C(C)=C1C.C[N-]C.C[N-]C.[Ti+2]
Reaction #43984
N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(3,5-dimethylphenyl)amine titanium bis(dimethylamide)
Ausbeute 222.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46153
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46154
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=NO
Reaction #46155
1-hydroxyimino-3-phenyl-6-(3-phenylpropyloxy)-1H-indene-2-carboxylate ethyl ester
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[NH-].O=C([O-])C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #46164
6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46174
title compound
Ausbeute 75.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O.[NH-]C1CCCCC1
Reaction #46175
title compound
Ausbeute 59.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #47807
titled compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1(O)c1ccccc1
Reaction #47808
titled compound
Ausbeute 113.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #47817
titled compound
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1Br
Reaction #47824
titled compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OC
Reaction #47825
titled compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1OCC
Reaction #47826
titled compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=NO
Reaction #47829
titled compound
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1N
Reaction #47830
titled compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1NC(C)=O
Reaction #47839
titled compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC1C(C(=O)OCC)=C(c2ccccc2)c2ccc(OC)cc21
Reaction #47841
titled compound
Ausbeute 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1N1CCOCC1
Reaction #47842
titled compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
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