Modified Phosphoramidites

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Identity (IR): passes test

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Identity (IR): passes test

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Identity (IR): passes test

Application Employed in a rhodium-catalyzed [3+2] annulation with alkynes leading to substituted indenones. Useful in the synthesis of substitutes indenones or indanones

May contain varying amounts of anhydride. Application Reactant involved in: Reactions with (cyanomethylphenyl)boronic acid Synthesis of oligo-boronic acid receptors with improved structural and electronic properties Syntesis of

May contain varying amounts of anhydride. Application Reactant involved in: Reactions with (cyanomethylphenyl)boronic acid Synthesis of oligo-boronic acid receptors with improved structural and electronic properties Syntesis of

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 4-Cyanophenylboronic acid can be used as a reactant in: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Ruthenium catalyzed direct arylation of benzylic sp 3 carbons of acyclic amines with arylboronates.

Application 4-Cyanophenylboronic acid can be used as a reactant in: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Ruthenium catalyzed direct arylation of benzylic sp 3 carbons of acyclic amines with arylboronates.

Diethyl(4-formylphenyl)phosphonate.

Diethyl(4-formylphenyl)phosphonate.

Diethyl(4-formylphenyl)phosphonate.