A one-pot, multistep reaction cascade to cyclopentenes from α, β-unsaturated ketones and
propargylated carbon acids through a combination of organocatalysis and transition metal …

DABCO-mediated isocyanide-based multicomponent reaction: synthesis of highly
substituted cyclopentenes - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C4OB00012A …

A copper-catalyzed cascade cyclization of enynes with Togni's reagent, carbon dioxide, and
amines has been successfully developed. The reaction provides a direct and efficient route …

Five‐membered carbocycles are ubiquitously found in natural products, pharmaceuticals,
and other classes of organic compounds. Within this category, cyclopentenes deserve …

CeCl3· 7H2O is found as an efficient catalyst for new intermolecular domino reactions of
three-, four-and seven-component assemblies of common precursors under benign reaction …

The stereocontrolled formation of medium-sized carbocycles is a major goal in modern
organic chemistry due to their widespread occurrence in natural products and …

A highly efficient and practical synergistically metal/proton‐catalyzed Conia–ene reaction for
the synthesis of bicyclo [3. n. 1] alkanones has been developed. This synergistic catalysis …

A highly selective cascade reaction that allows the direct transformation of dienallenes to
spirocyclobutenes (spiro [3.4] octenes) as single diastereoisomers has been developed. The …

We systematically investigated, for the first time, the relationship between regioselectivity
and acid/base effects in the cyclization reactions between carboxylic acids and carbon …

This work reports the construction of cyclopentene cores from 1, 6‐enynes and aryl diazo
ketones through two new reaction sequences involving initial gold‐catalyzed cyclization of …