Preparation of Heterocycles by Microwave-Induced Retro Diels-Alder Reaction

Title: Preparation of Heterocycles by Microwave-Induced Retro Diels-Alder Reaction

Volume: 3 Issue: 12

Author(s): Ferenc Miklos, Geza Stajer and Ferenc Fulop

Affiliation:

Keywords: Microwave, retro Diels-Alder reaction, N,N-, O,N-heterocycles

Abstract: Pyrimidinone, thioxopyrimidinone, pyrimido[2,1-a]phthalazinone and [1,3]oxazino[2,3-a] isoindolone were obtained by means of microwave-assisted [4+2] cycloreversion. The microwave heating of the parent norbornene or oxanorbornene fused compounds in a solvent with a medium or large loss factor generates retro Diels-Alder products in excellent yield and high purity.

Cite this article as:

Miklos Ferenc, Stajer Geza and Fulop Ferenc, Preparation of Heterocycles by Microwave-Induced Retro Diels-Alder Reaction, Letters in Organic Chemistry 2006; 3 (12) . https://dx.doi.org/10.2174/157017806779468086