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841034

O=C1c2ccccc2C(=O)N1CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #6812
3-phthalimidopropyltriphenylphosphonium bromide
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CC/C=C\c1cccc(Cl)c1
Reaction #6813
cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)C(=O)CN(C)C(=O)OC(C)(C)C.[Br-]
Reaction #86608
title compound
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CNCC(=O)N(C)CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.O=C([O-])C(F)(F)F
Reaction #86609
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)N(C)CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)C(=N)[NH3+].O=C([O-])C(F)(F)F.O=C([O-])C(F)(F)F
Reaction #86610
title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
[Br-]
Reaction #233890
DOI: 10.1039/C8SC04228D
CCOc1cc(C=C2CCN(C(N)=O)C2=O)ccc1O
Reaction #239201
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #268619
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCC=Cc1cccc(Cl)c1
Reaction #290290
DOI: 10.1039/C8SC04228D
COC(=O)Cc1ccc(OCc2ccccc2I)c(C=CCCN(C)C)c1
Reaction #292100
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #325345
[3-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl](triphenyl)phosphonium Bromide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cc2c(s1)/C(=C\CCN(C)C)c1ccccc1CC2.Cl
Reaction #330930
captioned compound
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C([P+](c2ccccc2)(c2ccccc2)c2ccccc2)CCN1CC(F)(F)F.[Br-]
Reaction #347185
Rac-[2-Oxo-1-(2,2,2-Trifluoroethyl)-Pyrrolidin-3-Yl]-Triphenyl-Phosphonium Bromide
DOI: 10.6084/m9.figshare.5104873.v1
[Br-]
Reaction #381134
DOI: 10.1039/C8SC04228D
CN1CCC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #393232
DOI: 10.1039/C8SC04228D
Br.CN(C)CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #451829
(3-dimethylaminopropyl)-triphenylphosphoniumbromide HBr
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1
Br.CCN(CC)CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #571959
(3-diethylaminopropyl)triphenylphosphonium bromide hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #597804
(3-(1,3-dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromide
Ausbeute 36.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CC/C=C\c1cccc(Cl)c1
Reaction #597805
(Z)-2-(4-(3-chlorophenyl)but-3-enyl)isoindoline-1,3-dione
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN1CCC([P+](c2ccccc2)(c2ccccc2)c2ccccc2)C1=O.[Br-]
Reaction #669669
rac-(1-Isobutyl-2-oxo-pyrrolidin-3-yl)-triphenyl-phosphonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
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