Reactions that utilize addition of active C− H nucleophiles to C X bonds represent some of
the most fundamental carbon− carbon bond-forming processes in organic chemistry. Of …

A comprehensive review of the publications about rosin-based chemicals has been
compiled. Rosin, or colophony, is a natural, abundant, cheap and non-toxic raw material …

Drug-lead synthesis through rapid construction of chiral molecular complexity around the
biologically relevant framework using a highly efficient strategy is a key goal of organic …

The full details of a catalytic asymmetric syn-selective nitro-Mannich reaction promoted by
heterobimetallic Cu/Sm/dinucleating Schiff base complexes are described, demonstrating …

For almost 20 years, thioureas have been experiencing a renaissance of interest with the
emerged development of asymmetric organocatalysts. Due to their relatively high acidity and …

Highly efficient: The title reaction provides biologically interesting chiral trifluoromethyl
dihydroquinazolinone frameworks in high yields (up to 97%) and with high …

A new family of bifunctional H-bond donor phase-transfer catalysts derived from cinchona
alkaloids has been developed and evaluated in the enantio-and diastereoselective nitro …

Easy to assemble! An enantioselective cascade Mannich intramolecular ring cyclization–
tautomerization reaction of malononitrile with 2‐hydroxyl N‐protected α‐amido sulfone is …

Thiourea-phosphonium salts from amino acids : cooperative phase-transfer catalysts in the
enantioselective aza-Henry reaction - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC42864H …

Due to the lack of tumor‐specific anticancer agents, the discovery and development of new
types of highly selective anticancer agents is still a very urgent topic. Herein, we present our …