cyclopropylmagnesium bromide

—
Reaction #6313
SiO2
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OC1(C2CC2)CCc2cc(F)ccc21
Reaction #41969
title compound
Ausbeute 106.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1Nc2ccc(Cl)cc2C(c2ccc(Br)cc2)(C2CC2)N1CC(F)(F)F
Reaction #47975
6-chloro-4-cyclopropyl-4-(4-bromophenyl)-3-(2,2,2-trifluoroethyl)-3,4-dihydroquinazolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1Nc2ccc(Cl)cc2C(C2CC2)(C(F)(F)F)N1CC(F)(F)F
Reaction #47985
6-chloro-4-cyclopropyl-3-(2,2,2-trifluoroethyl)-4-(trifluoromethyl)-3,4-dihydroquinazolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cc(Br)cc(C2CC2)c1
Reaction #48067
desired product
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #66631
residue
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1ccc2c(C3CC3)cccc2c1
Reaction #67024
1-cyclopropylnaphthalene
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)CCCCCCC1CC1
Reaction #72408
7-cyclopropylheptanoic acid
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1ccc(-c2cccc(Cl)c2)cc1C(O)(C1CC1)C1CC1
Reaction #78976
(4-Amino-3′-chloro-biphenyl-3-yl)-dicyclopropyl-methanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc(Nc2nc(COCC(F)(F)F)cc(C(O)C3CC3)n2)ccc1-n1cnc(C)c1
Reaction #87435
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1ncnn2c(CN3CCOCC3)c(C(=O)C3CC3)c(-c3ccc(NC(=O)Nc4cc(C(F)(F)F)ccn4)cc3)c12
Reaction #160879
above compound
Ausbeute 12.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccncc1N1CCN(c2ccc(C(O)C3CC3)c(F)c2)C1=O
Reaction #167390
product
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccncc1N1CCN(c2ccc(C(O)C3CC3)c(F)c2)C1=O
Reaction #167448
product
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)N2CCOCC2)cc1-c1cnc(N)c(C(=O)C2CC2)n1
Reaction #168646
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCCNS(=O)(=O)c1cccc(-c2cnc(N)c(C(=O)C3CC3)n2)c1
Reaction #168650
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #168951
residue
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OC1(C2CC2)c2ccccc2CCc2ccccc21
Reaction #321846
5-cyclopropyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
OC1(C2CC2)c2ccccc2C=Cc2ccccc21
Reaction #321848
5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
OC1(C2CC2)c2ccccc2Sc2ccccc21
Reaction #321850
9-cyclopropyl-9H-thioxanthen-9-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
O=C(c1ccc(C(F)(F)F)nc1)C1CC1
Reaction #329050
Cyclopropyl(6-(trifluoromethyl)pyridin-3-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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