A new linker design for solid phase synthesis has been developed that is cleaved under mild, neutral conditions using samarium(II) iodide. The feasibility of the linker approach has been illustrated in the solid phase synthesis of ketones and amides using an oxygen linker. Insights into the mechanism of the samarium(II) iodide cleavage reaction are described and the potential of a sequential cleavage carbon-carbon bond forming process is assessed. © The Royal Sociery of Chemistry 2005
930-936Samarium(II) iodide has been found to induce carbon-carbon bond cleavage in a number of bicy...
Abstract: This review article focuses on concepts that incorporate safety-catch and multiply cleavab...
Three efficient methods for synthesis of five membered carbocycles, a highly understudied product mo...
Exploring the potential of a new linker system cleaved using SmI2. The well known reduction of ?-het...
A sulfur α-heteroatom-substituted carbonyl (HASC) linker has been utilized in a solid-phase approach...
This thesis describes the development of methods using divalent samarium reagents in organic synthes...
In little more than twenty-five years, samarium(II) iodide (SmI 2) has become a benchmark reducing a...
Solid phase organic synthesis is a powerful technique to facilitate rapid synthesis and easy purific...
This review covers recent results in the area of solid phase organometallic chemistry during the per...
Samarium diiodide (SmI2) is one of the most widely used single-electron reductants available to orga...
Chemistry has been defined by some as an art, by others as a science and people have gone as far as ...
This thesis is concerned with the synthesis, and samarium diiodide mediated radical cyclisations of ...
Thesis (M.S., Chemistry)--California State University, Sacramento, 2013.Fused ring carbocycles conta...
This thesis is concerned with the synthesis, and samarium diiodide mediated radical cyclisations of ...
Linker strategies lie at the heart of solid phase and combinatorial chemistry. HASC (alpha-Hetero-At...
930-936Samarium(II) iodide has been found to induce carbon-carbon bond cleavage in a number of bicy...
Abstract: This review article focuses on concepts that incorporate safety-catch and multiply cleavab...
Three efficient methods for synthesis of five membered carbocycles, a highly understudied product mo...
Exploring the potential of a new linker system cleaved using SmI2. The well known reduction of ?-het...
A sulfur α-heteroatom-substituted carbonyl (HASC) linker has been utilized in a solid-phase approach...
This thesis describes the development of methods using divalent samarium reagents in organic synthes...
In little more than twenty-five years, samarium(II) iodide (SmI 2) has become a benchmark reducing a...
Solid phase organic synthesis is a powerful technique to facilitate rapid synthesis and easy purific...
This review covers recent results in the area of solid phase organometallic chemistry during the per...
Samarium diiodide (SmI2) is one of the most widely used single-electron reductants available to orga...
Chemistry has been defined by some as an art, by others as a science and people have gone as far as ...
This thesis is concerned with the synthesis, and samarium diiodide mediated radical cyclisations of ...
Thesis (M.S., Chemistry)--California State University, Sacramento, 2013.Fused ring carbocycles conta...
This thesis is concerned with the synthesis, and samarium diiodide mediated radical cyclisations of ...
Linker strategies lie at the heart of solid phase and combinatorial chemistry. HASC (alpha-Hetero-At...
930-936Samarium(II) iodide has been found to induce carbon-carbon bond cleavage in a number of bicy...
Abstract: This review article focuses on concepts that incorporate safety-catch and multiply cleavab...
Three efficient methods for synthesis of five membered carbocycles, a highly understudied product mo...