Phase‐transfer catalysis has been recognized as a powerful method for establishing
practical protocols for organic synthesis, because it offers several advantages, such as …

Die Phasentransferkatalyse bildet eine effiziente Grundlage zur Einführung praktischer
Methoden in die organische Synthese, denn sie bietet mehrere Vorteile wie einfache …

We describe the fully stereodivergent, dual catalytic α-allylation of linear aldehydes. The
reaction proceeds via direct iridium-catalyzed substitution of racemic allylic alcohols with …

We have developed a novel approach for the synthesis of enantioenriched 3-boryl-
tetrahydropyridines via the Cu (I)-catalyzed regio-, diastereo-, and enantioselective …

Decarboxylative cross-coupling methodologies are now widely employed in pharmaceutical
drug discovery research, forming the basis of strategic retrosynthetic analysis and radical …

The catalytic enantioselective synthesis of the chiral key intermediate of the antidepressant
(−)-paroxetine is demonstrated as a continuous flow process on multi-gram scale. The …

Fe-catalyzed direct dehydrogenative C (3)-functionalization of tertiary arylamines was
developed via activation of the sp3 C (3)–H bond. The reaction is applicable to both cyclic …

The selective synthesis of C-2/C-3 aminated five-membered heteroarenes incorporated
various functionalities with aniline derivatives in a sustainable way remains an unmet …

Non-aromatic nitrogen-and oxygen-containing heterocycles such as piperidines and pyrans
are prevalent components of natural products and pharmaceutical drugs. Although it has …

Recent applications of organocatalytic Michael and Friedel–Crafts reactions in
enantioselective synthesis of biologically active compounds: natural products …