All Outputs (3)

Polymer supported palladium N-heterocyclic carbene complexes: long lived recyclable catalysts for cross coupling reactions (2004)
Journal Article
Steel, P., & Teasdale, C. (2004). Polymer supported palladium N-heterocyclic carbene complexes: long lived recyclable catalysts for cross coupling reactions. Tetrahedron Letters, 45(49), 8977-8980. https://doi.org/10.1016/j.tetlet.2004.10.061

Polyrner supported palladium complexes, containing a pyridyl bis N-heterocyclic carbene ligand system derived from isonicotinic acid, provide highly stable catalysts for Heck and Suzuki cross coupling reactions. These heterogenous catalysts can be re... Read More about Polymer supported palladium N-heterocyclic carbene complexes: long lived recyclable catalysts for cross coupling reactions.

A simple solid phase diversity linker strategy using enol phosphonates (2004)
Journal Article
Campbell, I., Guo, J., Jones, E., & Steel, P. (2004). A simple solid phase diversity linker strategy using enol phosphonates. Organic and Biomolecular Chemistry, 2(19), 2725-2727. https://doi.org/10.1039/b411111g

Polymer bound lactam enol phosphonates can be easily generated using simple phenol on polystyrene resin. These stable, storable compounds can be released in a diversity cleavage strategy, using Suzuki cross coupling conditions, to provide 2-arylenami... Read More about A simple solid phase diversity linker strategy using enol phosphonates.

Stereochemistry of the reaction of Si-phenyl silenes with butadienes: elaboration of the silacycloadducts to provide a novel route to substituted lactones (2004)
Journal Article
Sanganee, M., Steel, P., & Whelligan, D. (2004). Stereochemistry of the reaction of Si-phenyl silenes with butadienes: elaboration of the silacycloadducts to provide a novel route to substituted lactones. Organic and Biomolecular Chemistry, 2(16), 2393-2402. https://doi.org/10.1039/b404175e

Silenes generated through a silyl-modified Peterson olefination procedure can be trapped with a range of alkyl butadienes via a [4+2] cycloaddition pathway to afford silacycles accompanied by variable amounts of competing ene, [2+2] and silene dimer... Read More about Stereochemistry of the reaction of Si-phenyl silenes with butadienes: elaboration of the silacycloadducts to provide a novel route to substituted lactones.