911482-75-2

Usage

Uses

Used in Chemical Synthesis:
2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane is used as a reagent in various chemical synthesis processes due to its reactivity and the presence of functional groups that can participate in a wide range of reactions. Its allylic group allows for reactions such as allylation, while the dioxaborinane ring can be involved in ring-opening reactions or serve as a precursor for other boron-containing compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane is used as a building block for the synthesis of boron-containing pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Material Science:
2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane is used as a precursor in the development of new materials with specific properties. Its reactivity and the presence of functional groups can be exploited to create materials with tailored characteristics, such as improved thermal stability, mechanical strength, or electrical conductivity.
Used in Catalysts:
In the field of catalysis, 2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane can be used as a catalyst or a catalyst precursor for various chemical reactions. Its reactivity and the presence of the allylic group and dioxaborinane ring make it suitable for promoting specific transformations, such as cross-coupling reactions or hydroboration reactions.

Upstream product

• 6336-44-3 allylboronic acid 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 81759-74-2 2-isopropoxy-5,5-dimethyl-1,3,2-dioxaborinane 

Downstream Products

• 62108-06-9 allylmethylbutyl carbinol 
• 745813-67-6 2-(pyridin-3-yl)pent-4-en-2-ol 

Relevant academic research and scientific papers

Construction of multiple, contiguous quaternary stereocenters in acyclic molecules by lithiation-borylation

Lithiation of carbamates followed by borylation provides a powerful method for the homologation of boron reagents. However, when applied to hindered systems (secondary carbamates with tBu-boronic esters) for the construction of two quaternary centers, thi

Practical and efficient applications of novel dioxaborolanes and dioxaborinanes in the synthesis of corresponding boronates and their use in the palladium-catalyzed cross coupling reactions

The syntheses of boronates derived from the reaction of dioxaborolanes and dioxaborinanes with either organolithium or organomagnesium reagents are investigated along with their subsequent use in the palladium cross coupling reaction. The intrinsic stability of these cyclic esters contributes to their facile reaction with both lithium and magnesium nucleophiles at mild and safe conditions. We have found that many of the reactions proceed at room temperature which is a significant improvement over the traditional routes which require cryogenic temperatures. The scope of these reactions and their practical application to large scale process synthesis is described.

NOVEL BORATE DERIVATIVES AND THEIR APPLICATIONS

Borates, compositions comprising chiral (cyclic and acyclic) and achiral (cyclic and acyclic) borates; chiral (cyclic and acyclic) and achiral (cyclic and acyclic) biborates; and methods for their synthesis. Additionally, a significantly improved synthetic protocol for the synthesis of wide range of boronates starting from borates or biborates and Grignard or organolithium reagents that can be used for kilo lab and commercial scale production.