90535-82-3

Usage

Uses

Used in Cardiovascular Applications:
NA is used as a medication for treating low blood pressure and shock, as it helps to increase heart rate and blood pressure during fight-or-flight responses.
Used in Neurological Applications:
NA is used as a medication for treating attention-deficit hyperactivity disorder (ADHD) and depression, as it plays a role in mood regulation, attention, and arousal.
Used in Stress Response:
NA is involved in the body's response to stress and danger, making it a crucial chemical in the body's stress response and having significant impacts on cardiovascular and neurological functions.

Upstream product

• 1240492-43-6 racemic 4,4,5,5-tetramethyl-2-((1S,2S)-2-phenylcyclopropyl)-1,3,2-dioxaborolane 
• 1240492-43-6 (+/-)-4,4,5,5-tetramethyl-2-((1S,2R)-2-phenylcyclopropyl)-1,3,2-dioxaborolane 
• 100-42-5 styrene 
• 119873-74-4 (E)-2-(phenyl)ethylenyldimethylsilanol 
• 4843-72-5 (E)-2-phenylethenyllithium 
• 1035952-86-3 1-<β-Chlor-aethoxy>-2-phenyl-cyclopropan, opt.-inakt. 

Downstream Products

• 146035-52-1 3,4,4-Triphenyl-butyraldehyde 

Relevant academic research and scientific papers

Exploiting the enantioselectivity of Baeyer-Villiger monooxygenases via boron oxidation

The enantioselective carbon-boron bond oxidation of several chiral boron-containing compounds by Baeyer-Villiger monooxygenases was evaluated. PAMO and M446G PAMO conveniently oxidized 1-phenylethyl boronate into the corresponding 1-(phenyl)ethanol (ee = 82-91%). Cyclopropyl boronic esters were also oxidized but with no enantioselectivity. β-Boryl carboxylic esters were not oxidized by any BVMOs.

Synthesis of cyclopropylsilanols by the Simmons-Smith reaction of alkenylsilanols and lithium alkenylsilanolates

Alkenylsilanols and the corresponding lithium silanolates prepared in situ by the reaction of cyclic siloxanes with alkenyllithiums are transformed to the corresponding cyclopropylsilanols under the Simmons-Smith reaction conditions. The obtained cyclopropylsilanols are further converted into the corresponding cyclopropanols by the Tamao oxidation.