Behera, Rakesh R. published the artcileHydrosilylation of Esters Catalyzed by Bisphosphine Manganese(I) Complex: Selective Transformation of Esters to Alcohols, Safety of Methyl decanoate, the main research area is alc diol preparation; Xantphos manganese complex preparation chemoselective hydrosilylation catalyst crystal structure; manganese catalyst chemoselective hydrosilylation ester.
A tricarbonylruthenium Xantphos complex I was prepared and characterized by X-ray crystallog.; in the presence of I, esters underwent chemoselective hydrosilylation with phenylsilane under neat conditions (followed by workup with base) to yield esters. Aryl, alkyl, and alkenyl mono- and dicarboxylates and lactones underwent chemoselective reduction to alcs. and diols; ketoesters underwent reduction to diols. Poly(1,6-hexanediol adipate) underwent hydrosilylation to 1,6-hexanediol.
Organic Letters published new progress about Aliphatic alcohols Role: SPN (Synthetic Preparation), PREP (Preparation). 110-42-9 belongs to class esters-buliding-blocks, name is Methyl decanoate, and the molecular formula is C11H22O2, Safety of Methyl decanoate.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics