The construction of carbon− carbon bonds, along with the creation of stereogenic carbon
centers, continues to be an appealing and demanding area of research, and processes in …

Since the rediscovery of proline in 2000 as catalyst in aldol reaction by List, Barbas and
Lerner and, soon after, the development of iminium catalysis by DWC MacMillan, the …

Carbazolespirooxindole derivatives were synthesized in a high-yielding, atypically rapid,
stereocontrolled Diels–Alder reaction catalyzed by a C 2-symmetric bisthiourea …

A simple highly versatile and efficient synthesis of 2, 4, 5-trisubstituted imidazoles is
achieved by three-component cyclocondensation of 1, 2-dicarbonyl compound, aldehyde …

Creating sequential one-pot combinations of multi-component reactions (MCRs) and multi-
catalysis cascade (MCC) reactions is a challenging task that has already emerged as a new …

General Methods: The 1H NMR and 13C NMR spectra were recorded at 400 MHz and 100
MHz, respectively. The chemical shifts are reported in ppm downfield to TMS (δ= 0) for 1H …

High‐yielding asymmetric synthesis of bioactive molecules with the aid of mild catalysis is
an efficient approach in reaction engineering. In the early days, synthetic chemists mainly …

Cyclic ketones react with (E)‐2‐nitroallylic acetates in the presence of catalytic pyrrolidine‐
thiourea, which affords bicyclic skeletons with four or five stereocenters in one single …

The asymmetric synthesis of functionalized 2‐amino‐2‐chromene derivatives with high
enantioselectivities via one‐pot tandem reactions of functionalized α, β‐unsaturated ketones …

This book covers the latest developments in asymmetric domino reactions, focussing on
those published in the last 6 years. These fascinating reactions have rapidly become one of …