Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions are important tools
which have constantly grown over several years. This review summarizes and highlights …

This review describes, in brief, the philosophy, vision and long-term research experience of
the senior author (DB) in the area of the Baylis–Hillman (BH)[also known as the Morita …

Phosphonium ylides are being reported here as a catalyst for the formation of thiazolidines
and 1, 3-thiazinanes from β-ketothioamides (which act as a three atom N, C, and S synthon) …

An operationally simple and efficient cascade approach to access a series of 1, 3‐
thiazinanes has been developed through intermolecular [3+ 3] heteroannulative coupling …

A one-pot synthetic method for indole/pyrrole-fused 1, 4-diazepanone scaffolds has been
developed. This method involves a sequential amide coupling/intramolecular aza-Michael …

Abstract The Morita–Baylis–Hillman (MBH) reaction has been the subject of a number of
significant earlier reviews and continues to enjoy widespread application as an intrinsically …

Chemoselectivity is an important issue frequently encountered while working over labile
precursors. Carbonyl compounds with a heteroatom at the β carbon are sensitive precursors …

A convenient one‐pot protocol for the synthesis of benzo‐fused and indole‐fused
indolizines from Baylis–Hillman acetates was developed. This strategy involves CuBr/tert …

An efficient one‐pot allylic alkylation of α‐enolic dithioesters (DTEs) with Morita‐Baylis‐
Hillman (MBH) acetates has been devised in ethanol at room temperature. The reaction …

Despite being a very useful C–C bond forming and highly applicative reaction, Morita–Baylis–
Hillman (MBH) reaction has been limited by its excessive slow reaction rate, including its …