Substructure Search

454258

Cl[Si](Cl)(Cl)Cc1ccccc1
Reaction #186641
DOI: 10.1039/C8SC04228D
CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C=Cc2cccc(-c3ccc(C)cc3)c2)cc1
Reaction #240692
DOI: 10.1039/C8SC04228D
CCCCCCCC[Si](Cl)(Cl)Cl
Reaction #241285
DOI: 10.1039/C8SC04228D
CCCC[P+](CCCC)(CCCC)Cc1ccccc1CCl.[Cl-]
Reaction #353181
2-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1cccc(CCl)c1.[Cl-]
Reaction #353182
3-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccc(CCl)cc1.[Cl-]
Reaction #353183
4-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccc(CBr)cc1.[Br-]
Reaction #353184
4-(Bromomethyl)benzyltri-n-butylphosphonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
[Br-]
Reaction #398528
DOI: 10.1039/C8SC04228D
O=C(O)CNC1=CCCCC1
Reaction #441410
N-carboxymethyl-3,4,5,6-tetrahydroaniline
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccccc1CCl.[Cl-]
Reaction #462201
2-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1cccc(CCl)c1.[Cl-]
Reaction #462202
3-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccc(CCl)cc1.[Cl-]
Reaction #462203
4-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccc(CBr)cc1.[Br-]
Reaction #462204
4-(Bromomethyl)benzyltri-n-butylphosphonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CC=CCCC1
Reaction #547584
2,3,4,7-Tetrahydro-azepine-1-carboxylic acid benzyl ester
Yield 56.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)/C=C/c2cccc(-c3ccc(C)cc3)c2)cc1.[Cl-]
Reaction #653098
(E)-tributyl[4-[3-(4-methylphenyl)cinnamamido]benzyl]-phosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccccc1CCl
Reaction #894742
DOI: 10.1039/C8SC04228D
CCCC[P+](CCCC)(CCCC)Cc1cccc(CCl)c1
Reaction #1039093
DOI: 10.1039/C8SC04228D
OCc1cc2c(c(Cl)n1)OCC=C2
Reaction #1053032
(8-chloro-2H-pyrano[2,3-c]pyridin-6-yl)methanol
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1
Reaction #1054045
product
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccccc1C(=O)OC.[Br-]
Reaction #1059738
o-methoxycarbonylbenzyltributylphosphonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
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