benzylmagnesium chloride

O=C(CCC(Cc1ccccc1)c1c[nH]c2ccccc12)CCC(Cc1ccccc1)c1c[nH]c2ccccc12
Reaction #980
ketone
収率 68.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(Cc2nc(Nc3cc(C4CC4)n[nH]3)c3ccccc3n2)cc1
Reaction #7701
(2-benzyl-quinazolin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(Cc2cccc(-c3nn4c(c3-c3ccnc5ccccc35)CCC4)n2)cc1
Reaction #8350
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C1=C(Cc2ccccc2)Cc2ccccc21
Reaction #12060
2-benzylindene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@H](NC(=O)OC(C)(C)C)C(=O)Cc1ccccc1
Reaction #41360
tert-Butyl N-[(2S)-3-oxo-4-phenyl-butan-2-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(OC)cc2C1(O)Cc1ccccc1
Reaction #47805
titled compound
収率 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(SC(=S)Cc1ccccc1)C(=O)O
Reaction #48459
title compound ( 20 )
収率 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CC(SC(=S)Cc1ccccc1)C(=O)O
Reaction #48460
title compound ( 21 )
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1c(NCC(=O)Cc2ccccc2)nc(-c2ccncc2)c(-c2ccc3ccccc3c2)c1=O
Reaction #62255
final product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(OCC)[PH](=O)Cc1ccccc1
Reaction #64729
benzyl(diethoxymethyl)phosphine oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1ccccc1NC(Cc1ccccc1)c1ccccc1
Reaction #69607
B3
収率 96.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)NC1(c2ccc(C(=O)Cc3ccccc3)cc2)CCC1
Reaction #70646
tert-butyl {1-[4-(phenylacetyl)phenyl]cyclobutyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)S(=O)NC1(Cc2ccccc2)CCC(Oc2ccc3c(c2)CCC(c2ccccc2)O3)CC1
Reaction #88059
2-methyl-propane-2-sulfinic acid [1-benzyl-4-(2-phenyl-chroman-6-yloxy)-cyclohexyl]-amide
収率 43.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(=CCCCO)CCCCc1ccccc1
Reaction #216976
title compound
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
Brc1ccc(Cc2ccccc2)cc1
Reaction #216978
title compound
収率 80.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(C)(C)OC(=O)NC1(c2ccc(C(=O)Cc3ccccc3)cc2)CC2(C1)OCCO2
Reaction #309157
tert-butyl {2-[4-(phenylacetyl)phenyl]-5,8-dioxaspiro[3.4]oct-2-yl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C1Nc2ccc(Cl)cc2C1(O)Cc1ccccc1
Reaction #321668
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
NC(Cc1ccccc1)(c1cc(F)cc(C(F)(F)F)c1)c1ccc(F)c(C(F)(F)F)c1
Reaction #325905
1-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethanamine
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)[S@@](=O)N[C@@](Cc1ccccc1)(c1ccc(F)cc1)c1cc(F)cc(OC(F)(F)C(F)F)c1
Reaction #325909
(R)—N—((S)-1-(3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl)-1-(4-fluorophenyl)-2-phenylethyl)-2-methylpropane-2-sulfinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1cc(C(O)Cc2ccccc2)ccc1F
Reaction #325947
1-(4-fluoro-3-methoxyphenyl)-2-phenylethanol
収率 60.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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