Organic thiocyanates are valuable biological moities and drug-building blocks. They can
also transform effectively into thioethers, thiols, alkynyl thioethers, and thiocarbamates in …

An unprecedented protocol for a Rh (III)-catalyzed [3+ 2] annulation from simple and readily
available enaminones and iodonium ylides has been developed. The novel strategy allows …

Abstract In 2014, the World Health Organization called drug resistance to antibiotics a “major
global threat”. Therefore, the ever‐increasing human need for new antibiotics with greater …

An efficient and environmentally friendly electrochemical synthesis of phosphorylated
oxindoles and indolo [2, 1-a] isoquinolin-6 (5 H)-ones mediated by readily available Cp2Fe …

We present the first example of electrocatalytic three‐component annulation–
iodosulfonylation of indole‐tethered 1, 6‐enynes with arylsulfonyl hydrazides and KI for …

An efficient, green and one-pot strategy for the concise synthesis of diverse selenyl imidazo
[2, 1-b] thiazinones from diselenides, acryloyl chlorides and 2-mercaptobenzimidazoles/2 …

Cycloalkanols ring‐opening transformation is one of the most valuable and wide area of
research. Among the numerous methods that have been developed, transition‐metal‐free …

The P450 monooxygenase TleB (CYP107E48) catalyzes intramolecular C–S bond
formation in a thiol-containing substrate, yielding two sulfur-containing indolactam …

An unexpected isomerization of azomethine ylides generated in situ from isatin with indoline-
2-carboxylic acid has been disclosed, providing direct access to N-functionalized indole …

In the pursuit of forging innovative electrosynthetic pathways and nurturing sustainable
chemical processes, an in-depth comprehension of the structure and reactivity of reactive …