This comprehensive review summarizes the published literature data concerning the
intramolecular Diels–Alder reactions of vinylarenes (the IMDAV reaction) and alkynyl arenes …

Diversely substituted, partially saturated benzo [f] isoindole-4-carboxylic acids were
synthesized by a new three-component reaction (3CR) starting from cinnamic amines (3 …

N-Furfuryl allylamines react with a broad range of isocyanates, isothiocyanates,
isoselenocyanates with the formation of a 3a, 6-epoxyisoindole core in one synthetic stage …

Abstract Interaction of 2-furylvinyl-and 2-thienylvinyl-2, 3-dihydroquinazolin-4 (1H)-ones with
maleic anhydride gives isoindolo [2, 1-a] quinazoline-11 (13)-carboxylic acids via the …

Intramolecular Diels–Alder vinylarene reaction (IMDAV) is a [4+ 2] cycloaddition that
employs styrene derivatives as conjugated dienes, whose poor reactivity arises from the …

N-Furfuryl allylamines, readily accessible from corresponding furfurals or furfuryl amines,
react with a broad range of arylsulfonyl chlorides with the formation of a 3a, 6 …

An efficient and highly selective reaction of 2‐(2‐bromophenyl)‐5, 6, 7, 8‐tetrahydrobenzo
[4, 5] thieno [2, 3‐d] pyrimidin‐4 (3H)‐one and terminal alkyne has been developed under …

In the title compound, C24H21NO3S, the cyclopentene ring adopts an envelope
conformation. In the crystal, molecules are linked by C—H⋯ π interactions, forming ribbons …

In the title compound, C22H19NO5S· C2D6OS, the central six-membered ring has a slightly
distorted boat conformation, while the fused pyrrolidine ring adopts an envelope …

We have developed an efficient approach toward the synthesis of functionalized
hexahydropyrano [3, 4-c] pyrrole-1, 6-diones from readily accessible 3-thienylsubstituted …