The influence of catalyst in reaction 53562-86-0

In addition to the literature in the link below, there is a lot of literature about this compound((S)-Methyl 3-hydroxybutanoate)Synthetic Route of C5H10O3, illustrating the importance and wide applicability of this compound(53562-86-0).

Synthetic Route of C5H10O3. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: (S)-Methyl 3-hydroxybutanoate, is researched, Molecular C5H10O3, CAS is 53562-86-0, about Stereoselective Synthesis of Premisakinolide A, the Monomeric Counterpart of the Marine 40-Membered Dimeric Macrolide Misakinolide A. Author is Nakamura, Ryoichi; Tanino, Keiji; Miyashita, Masaaki.

The first synthesis of protected premisakinolide A (I), the monomeric counterpart of misakinolide A, the marine 40-membered macrolide displaying potent activity against a variety of human carcinoma cell lines (no data), has been reported. The strategy was highlighted by a crucial coupling of a tetrahydropyran fragment and an alkynylaluminum reagent having a polypropionate chain, the highly stereoselective cross aldol reaction of segment A and segment B, and the stereospecific construction of the polypropionate structure based on original acyclic stereocontrol.

In addition to the literature in the link below, there is a lot of literature about this compound((S)-Methyl 3-hydroxybutanoate)Synthetic Route of C5H10O3, illustrating the importance and wide applicability of this compound(53562-86-0).

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics