bromide

CCOC(=O)CCC(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
Reaction #4556
ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COCC1N=C(C2(C)C=CC(CC(C)C)=CC2)OC1c1ccccc1
Reaction #6619
2-(1-methyl-4-isobutylphenyl)-4-methoxymethyl-5-phenyl-2-oxazoline
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Brc1cccc(Br)c1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #11164
phosphonium
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(Cl)c(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1Cl.[Br-]
Reaction #11168
phosphonium
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #11172
phosphonium
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1cccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1Cl.[Br-]
Reaction #11175
phosphonium
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c(Cl)c1.[Br-]
Reaction #11177
phosphonium
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1ccc(Cl)c(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1.[Br-]
Reaction #11179
phosphonium
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c(Cl)c1.[Br-]
Reaction #11180
phosphonium
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(Cl)c(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1.[Br-]
Reaction #11182
phosphonium
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc([N+](=O)[O-])ccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #11244
phosphonium
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)COc1ccc(Cl)cc1O
Reaction #11710
(4-chloro-2-hydroxy-phenoxy)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)[C@H](NCc1ccc(Br)cc1)C(=O)O
Reaction #40870
N-(4-bromobenzyl)-L-valine
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)[C@H](NCc1ccc(Br)cc1)C(=O)O
Reaction #40871
N-(4-bromobenzyl)-L-valine
収率 153.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #46477
Compound 151
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=Cc1ccccc1C(C)=O
Reaction #46937
o-vinyl acetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCO[C@@H]1C[C@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)N(C(c2ccccc2)c2ccccc2)C1
Reaction #49213
title compound
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC(C)Oc1ccc(C=COC)cc1
Reaction #50165
1-(2-methoxyethenyl)-4-(1-methylbutyloxy)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC=Cc1ccc(C(=O)OC)cc1
Reaction #50166
methyl 4-(2-methoxyethenyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCCCCCC1=CC(=O)CCC1
Reaction #51586
3-hexyl-2-cyclohexenone
収率 111.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
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