In recent years, para-quinone methides (p-QMs) have emerged as attractive and versatile
synthons in organic synthesis owing to their high reactivity. Consequently, p-QM chemistry …

An important strategy for the efficient generation of diversity in molecular structures is the
utilization of common starting materials in chemodivergent transformations. The most …

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 …

In the last few years, there has been an explosive growth in the area of para‐quinone
methide (p‐QM) chemistry. This boom is actually due to the unique reactivity pattern of p …

A chiral phosphoric acid-catalyzed approach constructing dihydrocoumarin motifs by the
addition of azlactones to para-quinone methides (p-QMs) was developed. The reaction …

This work describes the first enantioselective 1, 6-additions of azlactones to para-quinone
methides. In the presence of a chiral phosphoric acid, 1, 6-adducts were obtained in high …

The first cyclization of para-quinone methide derivatives with alkynes was established by
utilizing the [4+ 2] reaction of ortho-hydroxyphenyl-substituted para-quinone methides with …

A formal 1, 6-conjugated addition-mediated [4+ 1] annulation of ortho-hydroxyphenyl-
substituted para-quinone methides with sulfonium or ammonium bromides has been …

In contrast to the well‐established [3+ 2] cycloaddition reactions, the catalytic
enantioselective [3+ n](n≥ 3) cycloaddition reaction of activated isocyanides for the …

Intramolecular nucleophilic aromatic substitution (Truce–Smiles rearrangement) of the
anions of 2‐benzyl benzanilides leads to triarylmethanes in an operationally simple manner …