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 …

This review covers formal insertion reactions of diazo compounds into aldehydes for the
formation of ketones (C single bondH bond insertion) and homologated aldehydes (Csingle …

This paper describes a catalytic enantioselective route to synthesize functionalized all-
carbon quaternary acyclic systems via a boron Lewis acid-promoted formal C–C insertion of …

Ein katalytischer Zugang zu chiralen α‐Alkyl‐β‐ketoestern besteht in der Umsetzung von α‐
Alkyldiazoestern mit Aldehyden (siehe Schema). Die Titelreaktion ergibt hohe bis …

Preparation of ketones by insertion of diazo compounds into the formyl C–H bond of an
aldehyde is an attractive procedure, but use of structurally diverse diazo compounds is …

Tuberculosis is the deadliest infectious disease affecting humankind with a death toll of
approximately 1.7 million people in 2016. The increasing prevalence of multidrug‐resistant …

We report a short synthetic route for synthesizing 2, 3-substituted piperazine acetic acid
esters. Optically pure amino acids were efficiently converted into 1, 2-diamines that could be …

The transesterification process has attained more significant importance in synthesizing a
variety of commercial and non‐commercial β‐ketoesters using alcohols and variety of …

SnCl2 catalyzed three-component coupling of aniline, epoxide, and paraformaldehyde
resulted in the synthesis of 1, 3-oxazolidine derivatives. The reaction is simple and does not …

Mild, efficient and racemization-free synthesis of N-protected α, β-unsaturated γ-amino
esters with unprecedented high E-stereoselectivity is described. This method is found to be …