A microwave‐assisted desulfuration of readily available dithiocarbamates, formed in situ
from primary amines, leading to target isothiocyanates has been developed. This efficient …

Cyclonucleosides are a group of nucleoside derivatives which, in addition to the classical N-
glycosidic bond, have an additional covalent bond (linker, bridge) in their structure, which …

A number of alkyl, aryl and bifunctional isothiocyanates are obtained in moderate to high
yields (41–94%) in a two-step, one-pot reaction of the parent primary amines or their salts …

Thirty-three alkyl and aryl isothiocyanates, as well as isothiocyanate derivatives from esters
of coded amino acids and from esters of unnatural amino acids (6-aminocaproic, 4 …

Thioureas are frequently used in organocatalysis and typically rely on 3, 5‐bis
(trifluoromethyl) phenyl moieties motifs to enhance their catalytic activity. In this work, these …

An expedient, solvent-free, mild base catalyzed intermolecular cyclization reaction has been
developed to enable the one-pot synthesis of fourteen examples of cyclobutane-fused …

A solvent‐free organocatalyzed intermolecular cyclization reaction starting from β‐
substituted γ‐hydroxy‐α, β‐unsaturated esters and aryl isothiocyanates proceeds via an aza …

Three new phenolic derivatives, picraquanines A–C (1–3), along with 6 known ones 4–9
were obtained from the stems of Picrasma quassioides (D. Don) Benn. The new structures …

A unified approach to access Nβ-protected amino alkyl isothiocyanates using Nβ-protected
amino alkyl azides through a general strategy of Staudinger/aza-Wittig reaction is described …

Background: Sulfur-containing compounds are widespread among natural products and
bioactive substances, and also useful ligands in asymmetric catalysis. Objectives: In this …