An efficient microwave-assisted green transformation of fused succinic anhydrides into N-aminosuccinimide derivatives of bicyclo[2.2.2]octene in water
- 24 August 2005
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 7 (10) , 737-741
- https://doi.org/10.1039/b508446f
Abstract
A very efficient and clean green synthesis of highly substituted prochiral bicyclo[2.2.2]oct-7-enes, starting from bicyclo[2.2.2]oct-7-ene-2exo,3exo,5exo,6exo-tetracarboxylic acid 2,3∶5,6-dianhydrides and a variety of hydrazines, is described.Keywords
This publication has 21 references indexed in Scilit:
- Microwave-assisted direct transformation of amines to ketones using water as an oxygen sourceChemical Communications, 2005
- Microwaves in organic synthesis. Thermal and non-thermal microwave effectsChemical Society Reviews, 2005
- Controlled Microwave Heating in Modern Organic SynthesisAngewandte Chemie International Edition in English, 2004
- Transition‐Metal‐Free Suzuki‐Type Coupling ReactionsAngewandte Chemie International Edition in English, 2003
- NewsGreen Chemistry, 2003
- Solid-state synthesis of heterocyclic hydrazones using microwaves under catalyst-free conditionsPresented, in part, at the 5th Electronic Conference on Synthetic Organic Chemistry, (ECSOC-5), 1–30 September 2001, E0014, http://www.mdpi.org/ecsoc-5.htmGreen Chemistry, 2002
- Diels-Alder Cycloaddition of Highly Substituted Pyran-2-ones with Maleic AnhydrideHETEROCYCLES, 2002
- Catalyst-free reactions under solvent-free conditions: microwave-assisted synthesis of heterocyclic hydrazones below the melting points of neat reactantsChemical Communications, 2001
- Solvent-free organic synthesesGreen Chemistry, 1999
- Didehydroamino Acids (DDAA) and Didehydropeptides (DDP)Synthesis, 1988