Organocatalytic domino/cascade reactions provide a convenient method for the construction
of complex molecular structures bearing multiple stereocenters in a highly stereoselective …

Carbon− heteroatom bond formations are very important reactions in organic synthesis and
have attracted the interest of many synthetic organic chemists, leading them to develop new …

Abstract Due to the competing 1, 4‐addition reactions and the distance from the chirality
information, the construction of a remote stereogenic center via 1, 6‐addition reactions is …

In the area of asymmetric organocatalysis, significant effort has been dedicated during the
last decade to improve the performance of emblematic catalysts such as proline, as well as …

Abstract Suitably substituted enantioenriched 4‐aryl‐1, 4‐dihydro‐pyridines prepared by an
organocatalytic enantioselective Michael addition were oxidized with MnO2 into axially …

A method for the synthesis of substituted cycloalkanes was developed using diols and
secondary alcohols or ketones via a cascade hydrogen borrowing sequence. A non-noble …

Well‐developed asymmetric organocatalysis has been widely incorporated in various
cascade/tandem sequences, providing a simple access to structurally complex target …

The β-ketoester structural motif continues to intrigue chemists with its electrophilic and
nucleophilic sites. Proven to be a valuable tool within organic synthesis, natural product, and …

The rapid development of organic chemistry and catalysis has provided outstanding
chemical tools to build complex molecular architectures that were never possible before. In …

An iridium catalyzed method for the synthesis of functionalized cyclohexanes from methyl
ketones and 1, 5-diols is described. This process operates by two sequential hydrogen …