As a common and integral feature of many natural products, thiocarboxylates play an
important role in biologically or pharmaceutically active compounds. Thiocarboxylates often …

Attachment of a growing peptide chain to a glycylaminomethyl resin via a thioglycinamide
bond is compatible with Fmoc-chemistry solid-phase peptide synthesis. Subsequent S …

Green chemistry expresses an area of research developing from scientific discoveries about
pollution awareness and it utilizes a set of principles that reduces or eliminates the use or …

In this paper, we report an efficient synthetic method for thioester formation from sodium
thiosulfate pentahydrate, organic halides, and aryl anhydrides. In the one-pot two-step …

A one-pot synthesis of thioesters directly from carboxylic acids, N, N′-diphenylthiourea,
triethylamine, and primary alkyl halides is described. Microwave-assisted heating and a …

The first zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides is
described. Various thioamides were reacted with N-arylsulfonyl aziridines in the presence of …

Full article: The Reaction of Thioacids with α-Haloketones in Water: an Environmentally Green
Synthesis of Thioester Derivatives Skip to Main Content Taylor and Francis Online homepage …

(E ž S, Se, Te), that have been isolated from polar solvents in the presence of suitable
counter-cations. Although unbranched chain-like dianions in the range n ž 2–6 are the only …

We describe the use of readily available crosslinked poly (4‐vinylpyridine) supported
sodium thiobenzoate,[P4VP] SCOPh, in the suspended solution phase synthesis of S‐alkyl …

Full article: Solvent-Free Conversion of Thioamides to Thioesters Skip to Main Content Taylor
and Francis Online homepage Taylor and Francis Online homepage Log in | Register Cart …