Sharpless asymmetric dihydroxylation is an important reaction in the enantioselective
synthesis of chiral vicinal diols that involves the treatment of alkene with osmium tetroxide …

Abstract The Julia‐Kocienski (J‐K) olefination is a modified version of Julia‐Lythgoe
olefination. In this reaction, an aldehyde or ketone is coupled with heterocycle‐bearing …

Asymmetric total synthesis of cyclotetradepsipeptide beauveamide A has been achieved for
the first time. A macrolactamization strategy involving two possible sites has been explored …

The stereoselective synthesis of the northern hemisphere (C20–C41) of the purported
structure of the extremely potent anticancer natural product neaumycin B has been …

Stereoselective total synthesis of structurally intriguing antimalarial macrolide strasseriolide
A has been accomplished by adopting a convergent approach. The salient features of this …

The Yamaguchi reagent, based on 2, 4, 6-trichlorobenzoyl chloride (TCBC) and 4-
dimethylaminopyridine (DMAP), is an efficient tool for conducting the intermolecular …

A convergent route for the asymmetric total synthesis of antibacterial macrolide sorangiolide
A has been developed for the first time. The key feature of this synthesis includes Krische …

A convergent strategy for the stereoselective synthesis of the methyl ester of the structurally
challenging and highly labile antibacterial polyene polyketide natural product thailandamide …

A convergent strategy for the first total synthesis of the lipopeptide bacilotetrin C has been
developed. The key features of this synthesis include Crimmins acetate aldol, Steglich …

A convergent route for the asymmetric total synthesis of potent anticancer polyketide natural
product amphirionin-2 has been developed. Our initial synthetic trials revealed that the …