Asymmetric catalysis with chiral metal complexes has received considerable attention in
recent years, and its contribution to the art of organic synthesis has become of leading …

The introduction of nitrogen atoms into small molecules is of fundamental importance and it
is vital that ever more efficient and selective methods for achieving this are developed. With …

Organoboronates represent a cornerstone functional group in modern synthesis owing to
their unique reactivity and divergent synthetic capability. Copper catalysis has become one …

Two-or one-electron-mediated difunctionalizations of internal alkenes represent
straightforward approaches to assemble molecular complexity by the simultaneous …

We have developed a copper-catalyzed enantioselective intermolecular aminoarylation of
alkenes using a novel N-fluoro-N-alkylsulfonamide as the amine reagent, which could react …

A method for the catalytic enantioselective arylboration of alkenylarenes is disclosed. The
reaction leads to the formation of 1, 1‐diarylalkanes that also incorporate an additional …

A palladium-catalyzed stereospecific and regioselective cross-coupling of enantiopure 2-
arylaziridines with arylboronic acids under mild conditions to construct a tertiary stereogenic …

A highly regioselective Lewis acid-mediated SN2-type ring-opening of N-sulfonylaziridines
and azetidines with tetraalkylammonium halides in CH2Cl2 solution to afford 1, 2-and 1, 3 …

The synthesis and reactions of epoxides and aziridines has been regularly reviewed. 1 e6
The most typical reaction of both heterocyclic systems is the ring-opening reaction in which a …

An efficient strategy for the synthesis of 3-(3-indolyl)-oxindole-3-methanol has been
developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro …