A catalytic domino spirocyclization of 1, 7-enynes with simple cycloalkanes and cyclo-1, 3-
dicarbonyls has been established via multiple C–C bond formations from alkynyl/alkenyl …

We report the convergent synthesis of bicyclo [3.1. 0] hexanes possessing an all-carbon
quaternary center via a (3+ 2) annulation of cyclopropenes with cyclopropylanilines. Using …

The [2+ 2+ 2] cycloaddition reaction is a useful tool to realize unusual chemical
transformations which are not achievable by traditional methods. Here, we report our work …

Transition metal-catalyzed carbocyclization reactions represent powerful methods for the
construction of complex polycyclic systems. We have developed a regiospecific and …

ipso-Annulation represents an attractive approach to synthesize a variety of spirocyclic
compounds having a quaternary carbon center. Furthermore, these compounds also serve …

A formal 1, 6-conjugated addition-mediated [2+ 1] annulation to synthesize spiro [2.5] octa-4,
7-dien-6-one with p-quinone methides and sulfur ylides has been described. This domino …

Cycloarenes are an essential class of polycyclic aromatic hydrocarbons with unique
electronic structure, but their synthesis is very challenging. Herein, we report a facile …

Spirooxindoles are privileged scaffolds in diverse bioactive natural products and
pharmaceuticals, significant achievements for the construction of these molecules have thus …

An unprecedented umpolung spirocyclopropanation reaction of p-quinone methides and α-
keto carbonyls is described. Our umpolung strategy based on 1, 6-conjugate addition and …

A Lewis acid catalyzed intramolecular [3+ 2] cross cycloaddition of cobalt-
alkynylcyclopropane 1, 1-diesters with carbonyls has been successfully developed …