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Nucleophilic Add.

Classic Method

Organolithium reagents are synthetically useful because they are great nucleophiles, strong bases, and effective catalysts for radical and anionic polymerizations. However, they often catch fire in the presence of air. To control these hazards, they are dissolved at low concentrations in ether solutions, which lessen the hazards, but are themselves dangerous.

ButylLithium Addition

Problems

  • Must be stored at cold temperatures to prevent decomposition
  • Available only at low concentrations in ether
  • Little selectivity and significant solvent waste
  • Many organolithiums are not commercially available and must be prepared at time of use

SiGNa’s Method

The SiGNa organolithium materials provide an extensive suite of nucleophiles that do not suffer from many of the traditional limitations. The SiGNa method increases selectivity and yield, while easing process setup, separation, and workup.

ButylLithium Addition

AllylLithium Addition

BenzylLithium Addition

Benefits

  • Allows for a smooth solution process in batch or continuous-flow reactors
  • SiGNa’s nucleophilic reagents are dry powders storable at room temperature for indefinite lengths of time
  • No highly flammable or hazardous solvents required
  • Increased selectivity and control of reaction

Recommended Products for Nucleophilic Addition

Organolithium-Alumina Gel

Bottle-able solid powdery reagent loaded up to 10 mmol/g; storable under nitrogen with infinite shelf life; extended range of organolithium nucleophiles

New Discoveries

Currently SiGNa is working on the next element in the alkali metal family, Lithium. A number of new discoveries have been made. Read More

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