Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Microwave pericyclic reactions

This chapter has taken the reader through a number of microwave-assisted methodologies to prepare and further functionalize 2-pyridone containing heterocycles. A survey of inter-, intramolecular-, and pericyclic reactions together with electrophilic, nucleophilic and transition metal mediated methodologies has been exemplified. Still, a number of methods remain to be advanced into microwave-assisted organic synthesis and we hope that the smorgasbord of reactions presented in this chapter will inspire to more successful research in this area. [Pg.27]

The best solvent from an ecological point of view is without doubt no solvent. There are many great reactions that can already be carried out in the absence of a solvent, for example numerous industrially important gas-phase reactions and many polymerizations. Diels-Alder and other pericyclic reactions are also often carried out without solvents. Reports on solvent-free reactions have, however, become increasingly frequent and specialized over the past few years. Areas of growth include reactions between solids [5], between gases and solids [6], and on supported inorganic materials [7], which in many cases are accelerated or even made possible through microwave irradiation [8]. [Pg.82]

Choshi, T., Kumemura, T., Nobuhiro, J., and Hibino, S. 2008. Novel synthesis of the 2-azaanthraquinone alkaloid, scorpinone, based on two microwave-assisted pericyclic reactions. Tetrahedron Letters, 49 3725-28. [Pg.207]

Soares, M.I.L., Teresa M.V.D., and Melo, P. 2008. Microwave-assisted generation and reactivity of aza- and diazafulveniummethides Heterocycles via pericyclic reactions. Tetrahedron Letters, 49 4889-93. [Pg.211]

In a series of publications over the past few years, the group of Barriault has reported on microwave-assisted tandem oxy-Cope/Claisen/ene and closely related reactions [175-178], These pericyclic transformations typically proceed in a highly stereoselective fashion and can be exploited for the synthesis of complex natural products possessing decalin skeletons, such as the abietane diterpene wiedamannic... [Pg.165]


See other pages where Microwave pericyclic reactions is mentioned: [Pg.683]    [Pg.163]    [Pg.168]    [Pg.179]    [Pg.211]    [Pg.114]    [Pg.149]    [Pg.7]    [Pg.10]    [Pg.132]    [Pg.282]    [Pg.211]   
See also in sourсe #XX -- [ Pg.178 , Pg.179 , Pg.180 , Pg.181 , Pg.182 , Pg.183 ]




SEARCH



Pericyclic

Pericyclic reactions

© 2024 chempedia.info