The catalysis by primary and secondary amines of electrophilic substitution reactions in the
R-position of carbonyl compounds and related reactions via enamine intermediates is called …

Vinyl sulfones have long been known for their synthetic utility in organic chemistry, easily
participating in 1, 4‐addition reactions and cycloaddition reactions. This functional group …

In this communication, we describe the development of the first highly enantioselective
catalytic conjugate addition to vinyl sulfones. Promoted by readily accessible …

Chiral framework: Chiral amines with pyrrolidine frameworks catalyze the enantioselective
conjugate addition of a wide range of aldehydes to various vinyl sulfones and vinyl …

The bifunctional thiourea–tertiary amine derivatives of simple chiral diamines serve as
highly enantioselective catalysts for the Michael addition of α-substituted cyanoacetates to …

Since its inception in 1945, this serial has provided critical and integrating articles written by
research specialists that integrate industrial, analytical, and technological aspects of …

A comprehensive review of recent chemistry of α, β-unsaturated sulfoxides and sulfones is
presented. Emphasis has been placed on new reactions and strategies, stereo-and enantio …

Since the publication of the review article entitled ''Multiply convergent syntheses via
conjugate-addition reactions to cycloalkenyl sulfones''about two decades ago, 1 a, b …

Unsaturated carbohydrate derivatives are useful intermediates in synthetic transformations
leading to a variety of compounds. The aim of this review is to highlight the rich chemistry of∆ …

Suitably designed vinyl sulfone-modified furanosides act as substrates for Michael initiated
ring closure reactions yielding cyclopropanated carbohydrates. The strategy is general in …