315248-77-2

Usage

Uses

Used in Pharmaceutical Research:
4-Pyrrolidin-2-ylhepta-1,6-dien-4-ol is utilized as a research compound for studying opioid receptors and their role in pain management. Its potent agonist activity on the mu-opioid receptor makes it a valuable tool for understanding the mechanisms of action and potential therapeutic applications of opioids.
Used in Drug Development:
In the field of drug development, 4-PIB serves as a reference compound for the design and synthesis of novel analgesic medications. Researchers aim to develop safer and more effective pain relief options with reduced potential for abuse and addiction compared to existing opioids.
Used in Forensic Toxicology:
4-Pyrrolidin-2-ylhepta-1,6-dien-4-ol is also relevant in forensic toxicology, where it is analyzed to identify and quantify the presence of this substance in biological samples. This is crucial for law enforcement and public health officials in addressing the potential for abuse, overdose, and the associated risks to public safety.
Used in Public Health and Policy Making:
The study of 4-Pyrrolidin-2-ylhepta-1,6-dien-4-ol contributes to public health and policy making by providing insights into the risks and consequences of synthetic opioid abuse. This information is essential for developing strategies to prevent addiction, improve treatment options, and reduce the overall impact of the opioid crisis on society.

Upstream product

• 688-61-9 Triallylborane 
• 147-85-3 L-proline 
• 2133-40-6 L-proline methyl ester monohydrochloride 
• 1730-25-2 allylmagnesium bromide 
• 106-95-6 allyl bromide 

Relevant academic research and scientific papers

L-proline-derived dendritic tetrakis(diperoxotungsto)phosphate: Synthesis and enantioselective oxidation catalysis

As a part of our ongoing research towards the synthesis of chiral dendritic polyoxometalate (DENDRI-POM) hybrids that are able to catalyze oxidation of organic substrates with high selectivity and enantioselectivity, we have prepared an enantiopure DENDRI-POM salt by coupling a well-defined L-proline-derived tetrapropylammonium dendron with the tetrakis(diperoxotungsto) phosphate [PO4{WO(O2)2}4] 3-. This DENDRI-POM hybrid was characterized by infrared, NMR spectroscopy, polarimetry, and elemental analysis. The data obtained are consistent with the structure in which the trianionic POM is surrounded by three L-proline-based dendrons. This DENDRI-POM oxidized sulfides with moderate activity and very low enantioselectivities (up to 4 %), whereas alkenes were efficiently oxidized with up to 37 % enantiomeric excess (ee), and good yields. Although these ee values are still not satisfactory for practical asymmetric synthesis, 37 % ee represents the best enantioselectivity reported to date in the oxidation of organic substrate with chiral POM hybrids. Studies of temperature, solvent, and catalyst loading effects on the outcome of the reaction indicate that the ee is sensitive to the nature of the solvent. Moreover, the catalyst was recovered at low temperature and reused while retaining its activity and enantioselectivity. These results contrast and complement our reported results in which DENDRI-POMs based on phenylethylamine-derived ligands efficiently oxidize sulfides with up to 14 % ee, whereas alkenes were not oxidized with this family of chiral POM compounds. Thus, the influence of the nature of the chiral countercation on the POM properties is again observed. L-Proline-derived dendritic tetrakis(diperoxotungsto)phosphate was prepared byassembling enantiopure L-proline-derived ligands with the anionic polyoxometalate (POM) unit. This DENDRI-POM catalyzes the oxidation of alkenes to the corresponding epoxides with 37 % ee. This ee value is the best enantioselectivity reported to date in the oxidation of organic substrates with chiral POM hybrids. Copyright

Diethylzinc: A simple and efficient catalyst for the swift hydroamination at room temperature

Diethylzinc and dimethylanilinium tetrakis(pentafluorophenyl)borate were found to catalyze hydroaminations at room temperature in high efficiency and very short reaction times. The reactivity of the proposed cationic zinc species, which is assumed to cata

Reductive diallylation of natural amino acids with triallylborane. The first synthesis of chiral 1,1-diallyl-2-amino alcohols and their cyclization into optically active pyrrolidines

The titled amino alcohols are obtained by treatment of chiral amino acids with triallylborane. Electrophylic iodocyclization of the alcohols leads to pyrrolidine derivatives.