Visible‐light‐induced radical decarboxylative functionalization of carboxylic acids and their
derivatives has recently received considerable attention as a novel and efficient method to …

The direct application of carboxylic acids as a traceless activation group for radical Michael
additions has been accomplished via visible light-mediated photoredox catalysis. Photon …

This review outlines the most recent papers describing the stereoselective synthesis of γ-
amino acids. In this update, the γ-amino acids have been classified according to the type of …

Cross-coupling of two alkyl fragments is an efficient method to produce organic molecules
rich in sp 3-hybridized carbon centres, which are attractive candidate compounds in drug …

This review covers recent advances in decarboxylative photocatalysis applicable to the
medicinal chemist. The review is not intended to be exhaustive, but instead is focussed on …

Der radikalischen decarboxylierenden Funktionalisierung von Carbonsäuren und ihren
Derivaten mithilfe von sichtbarem Licht wird seit einiger Zeit erhöhte Aufmerksamkeit zuteil …

Tetrahydro-β-carboline skeletons are prominent and ubiquitous in an extraordinary range of
indole alkaloid natural products and pharmaceutical compounds. Powerful synthetic …

Our current unhealthy lifestyle and the exponential surge in the population getting affected
by a variety of diseases have made pharmaceuticals or drugs an imperative part of life …

An alternate synthesis of appetite suppressant (R)-2-benzylmorpholine employing Sharpless
asymmetric epoxidation strategy - ScienceDirect Skip to main contentSkip to article Elsevier …

An alternative highly enantioselective synthesis of the anti-Parkinson agent safinamide from
simple, commercially available, starting materials is described. The protocol might also be …