Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 72824-04-5, formula is C9H17BO2, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , HPLC of Formula: 72824-04-5
Gao, Yaru;Wang, Luo-Yu;Zhang, Tao;Yang, Bin-Miao;Zhao, Yu research published 《 Atroposelective Synthesis of 1,1′-Bipyrroles Bearing a Chiral N-N Axis: Chiral Phosphoric Acid Catalysis with Lewis Acid Induced Enantiodivergence》, the research content is summarized as follows. Herein a highly efficient atroposelective synthesis of axially chiral 1,1′-bipyrroles such as I [R1 = Ph, 2-furyl, 2-naphthyl, etc.; R2 = CO2Me, CO2Et, CO2t-Bu, CO2allyl, CO2Bn; R3 = Me, Et] bearing an N-N linkage from simple hydrazine and 1,4-diones was presented. Further product derivatizations led to axially chiral bifunctional compounds with high potential in asym. catalysis. For this chrial phosphoric acid (CPA)-catalyzed double Paal-Knorr reaction, an intriguing Fe(OTf)3-induced enantiodivergence was also observed
HPLC of Formula: 72824-04-5, Allylboronic acid pinacol ester is a useful research compound. Its molecular formula is C9H17BO2 and its molecular weight is 168.04 g/mol. The purity is usually 95%.
Allylboronic acid pinacol ester is an allylation reagent that is used to produce aldehydes from ketones. It reacts with water, yielding the desired product and formaldehyde as a byproduct. The reaction proceeds through a sequence of steps, in which the boronate ester first reacts with water to form an allylboronate ion and hydrogen gas. This intermediate then reacts with potassium t-butoxide to produce the desired allyl alcohol and potassium borohydride. Finally, the palladium complex catalyst reduces the carbonyl group of the starting material, converting it into an aldehyde. Allylboronic acid pinacol ester is commercially available as a white solid, but can also be synthesized from 2-chloro-5-pinacolylborane (pinacol) in high yield using catalytic cross coupling reactions., 72824-04-5.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts