The Origin of the Halogen Effect on Reactivity and Reversibility of Diels–Alder Cycloadditions Involving Furan
- 13 February 2006
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 118 (9) , 1470-1473
- https://doi.org/10.1002/ange.200502677
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Derivatives of 7-oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediatesTetrahedron, 1999
- Synthetic applications of furan Diels-Alder chemistryTetrahedron, 1997
- Pseudo‐Spherical Host Molecules: Synthesis, Dimerization, and Nucleation EffectsAngewandte Chemie International Edition in English, 1995
- Pseudokugelförmige Wirtmoleküle: Synthese, Dimerisierung und „Keimbildungseffekte”︁Angewandte Chemie, 1995
- Synthesis of a Fully Unsaturated“Molecular Board”Angewandte Chemie International Edition in English, 1994
- Synthese eines vollständig ungesättigten „molekularen Brettes”︁Angewandte Chemie, 1994
- Molecular LEGO. 1. Substrate-directed synthesis via stereoregular Diels-Alder oligomerizationsJournal of the American Chemical Society, 1992
- Total synthesis of (.+-.)-dimethyl jaconateThe Journal of Organic Chemistry, 1988
- Five-membered heteroaromatic rings as intermediates in organic synthesisChemical Reviews, 1986
- Total synthesis of (.+-.)-nemorensic acidJournal of the American Chemical Society, 1985