Access to Unexplored 3D Chemical Space: cis-Selective Arene Hydrogenation for the Synthesis of Saturated Cyclic Boronic Acids was written by Kaithal, Akash;Wagener, Tobias;Bellotti, Peter;Daniliuc, Constantin G.;Schlichter, Lisa;Glorius, Frank. And the article was included in Angewandte Chemie, International Edition in 2022.Product Details of 1132669-90-9 The following contents are mentioned in the article:
A new class of saturated boron-incorporated cyclic mols. has been synthesized employing an arene-hydrogenation methodol. Cis-Selective hydrogenation of easily accessible, and biol. important mols. comprising benzoxaborole, benzoxaborinin, and benzoxaboripin derivatives is reported. Among the various catalysts tested, rhodium cyclic(alkyl)(amino)carbene [Rh-CAAC] (1) pre-catalyst revealed the best hydrogenation activity confirming turnover number up to 1400 with good to high diastereoselectivity. A broad range of functional groups was tolerated including sensitive substituents such as -F, -CF3, and -silyl groups. The utility of the synthesized products was demonstrated by the recognition of diols and sugars under physiol. conditions. These motifs can have a substantial importance in medicinal chem. as they possess a three-dimensional structure, are highly stable, soluble in water, form hydrogen bonds, and interact with diols and sugars. This study involved multiple reactions and reactants, such as 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9Product Details of 1132669-90-9).
5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Product Details of 1132669-90-9
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem