The Kabachnik–Fields reaction, comprising the condensation of an amine, oxo compound
and a P-reagent (generally a> P (O) H species or trialkyl phosphite), still attracts interest due …

2-Alkynylbenzamides underwent different reaction pathways when allowed to react under
PdI2-catalyzed oxidative carbonylation conditions, depending on the nature of the external …

N-Alkyl and N-aryl-isoindolinones were prepared by a dioxane-mediated oxidation of
isoindoline precursors. The transformation exhibits unique chemoselectivity for …

Practical and high stereoselective synthesis of 3-(arylmethylene) isoindolin-1-ones is
reported. The synthetic method involves the preparation of dimethyl isoindolin-1-one-3-yl …

In this work, efficient synthesis of isoindolin‐1‐one‐3‐phosphonates under catalyst‐and
solvent‐free conditions was reported to afford the desired compounds in excellent yields …

A simple and efficient microwave (MW)-assisted method was elaborated for the catalyst-free
synthesis of isoindolin-1-one-3-phosphonates by the three-component condensation of 2 …

An efficient and mild three-component synthesis of isoindolin-1-one-3-phosphonates is
described. The reaction between a 2-formylbenzoic acid, a primary amine, and a trialkyl …

Several multicomponent synthetic approaches were elaborated for plenty of novel nitrogen
or oxygen heterocycles containing a phosphonate or a phosphine oxide moiety. All …

A new method for the synthesis of 3-oxoisoindolin-1-ylphosphine oxides bearing same or
different substituents on the phosphorus atom is described. The one-pot three-component …

A facile and efficient method for the synthesis of N-substituted isoindolin-1-one derivatives
from 2-formylbenzoic acid and amine under Pd (OAc) 2/HCOOH system has been …