540293
Tetraalkylammonium carbonate, polymer-bound
macroporous, 40-90 mesh, extent of labeling: 2.5-3.5 mmol/g loading
Synonym(s):
MP-carbonate resin
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About This Item
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form
macroporous
reaction suitability
reaction type: solution phase peptide synthesis
reactivity: proton reactive
extent of labeling
2.5-3.5 mmol/g loading
particle size
40-90 mesh
SMILES string
[O-]C([O-])=O.C=Cc1ccccc1.C=Cc2ccc(C=C)cc2.CC[N+](CC)(CC)Cc3ccccc3.CC[N+](CC)(CC)Cc4ccccc4
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Application
Polymer-bound tetraalkylammonium carbonate is a polymer-supported base used for scavenging acidic molecules. It can be used in polymer-assisted solution-phase (PASP) Suzuki reactions.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Ley, S.V. et al.
J. Chem. Soc., Perkin Trans., 1251-1251 (1999)
Recent applications of polymer-supported reagents and scavengers in combinatorial, parallel, or multistep synthesis.
Thompson L A.
Current Opinion in Chemical Biology, 4(3), 324-337 (2000)
Polymer-assisted solution-phase (PASP) Suzuki couplings employing an anthracene-tagged palladium catalyst.
Lan P, et al.
The Journal of Organic Chemistry, 68(25), 9678-9686 (2003)
Parlow, J. et al.
Tetrahedron Letters, 38, 7959-7959 (1999)
S R Stauffer et al.
Journal of combinatorial chemistry, 2(4), 318-329 (2000-07-13)
Most ligands for the estrogen receptor (ER) are not well suited for synthesis by combinatorial means, because their construction involves a series of carbon-carbon bond forming reactions that are not uniformly high yielding. In previous work directed to overcoming this
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