A highly regioselective divergent approach is reported for the synthesis of both indeno [2, 1-
c] pyran-3-one and 1-oxazolonylisobenzofuran derivatives using the Erlenmeyer–Plöchl …

Easy access to N-aryl, N-heteroarylbenzoxazolinones and 4-aza analogues via Diels–Alder
cycloaddition reactions - ScienceDirect Skip to main contentSkip to article Elsevier logo …

An efficient and concise method was developed for access to indenofurans and
indenopyridines through a one pot, three-component protocol from heterocyclic ketene …

A Lewis acid initiated intramolecular cyclization of benzylidene acetal with an azide functional
group: novel synthesis of oxazolines and oxazines - Chemical Communications (RSC …

Organic azide cyclization reactions with 1-aryl allylic alcohols were investigated in a
synthetic study of phenanthroindolizidine alkaloids. Unsaturated imines (enimines) were …

Alkynylaryl aldehydes are widely used in organic reactions. Their great success is rooted in
their multiple functional groups. This review will focus on five kinds of triggered …

An efficient protocol for the chemoselective construction of the indeno [1, 2-b] pyrroles and
rearranged indeno [1, 2-b] pyrrole derivatives is reported via an N-acylation/cyclization/Wittig …

A novel bicyclization of 2-(2-(hydroxymethyl)-1-methylene-2, 3-dihydro-1H-inden-2-yl)
ethanol with aldehydes in the presence of 10 mol% BF3· OEt2 in dichloromethane at 0–25° …

A method for the preparation of novel oxaza and diaza polycyclic 9-oxa-4-azaphenanthrene,
5 H-pyrido [2, 3-a] pyrrolizine, 5 H, 6 H-pyrido [3, 2-g] indolizine, and 5 H, 6 H-indeno [2, 1-a] …

An efficient and one-pot procedure for the synthesis of arylated and stereodefined allylic
alcohols has been achieved through zirconium-mediated multicomponent coupling …