para‐Quinone methides (p‐QMs) are naturally occurring molecules that have been finding
increasing synthetic applications in the last few years. The presence of two electronically …

The last couple of decades has witnessed an incredible development in the progress of
catalytic creation of triarylmethane (TRAM) motif. The broad‐spectrum applications of …

A catalytic asymmetric conjugate addition of indoles to o-hydroxyphenyl substituted p-
quinone methides has been established in the presence of chiral phosphoric acid, which …

Chiral dihydrobenzofuran units are frequently present in molecules with significant
biological and pharmaceutical activities. Herein, we present the first enantioselective formal …

Here, a catalyst-controlled chemodivergent 1, 6-addition of p-quinone methides with alkynes
was developed, affording diverse alkynyl-and vinyl-substituted diarymethanes. In this …

A BINOL-based chiral phosphoric acid was employed as an efficient catalyst in
enantioselective cycloaddition of ortho-hydroxyphenyl-substituted para-quinone methides …

This chapter covers the literature published during 2017 relating to the synthesis, the
reactivity and the application of phosphines, excluding the chemistry of their metal …

The first copper hydride (CuH)-catalyzed asymmetric 1, 6-conjugate reduction of p-quinone
methides is reported. This protocol provides a new method to access a variety of …

A novel chiral biamide–phosphine multifunctional catalyst has been developed that
mediates the asymmetric intermolecular Michael addition of β-carbonyl esters to β …

The enantioselective conjugate addition of 2-naphthols to ortho-hydroxyphenyl substituted
para-quinone methides has been achieved with the aid of a chiral phosphoric acid …