Tandem Enyne Metathesis-Diels—Alder Reaction for Construction of Natural Product Frameworks.
✍ Scribed by Marta Rosillo; Gema Dominguez; Luis Casarrubios; Ulises Amador; Javier Perez-Castells
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 265 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
An Expedient Route for the Stereoselective Construction of Bridged Polyheterocyclic Ring Systems Using the Tandem "Pincer" Diels-Alder Reaction. -The tandem Diels-Alder reaction of furans with acetylenes is found to proceed regio-and stereoselectively as well as chemoselectively. Reactions using th
Natural Products Synthesis by retro-Diels-Alder Reactions. Part 15. Using a Rigid Molecule Tricyclodecadienone for the Stereospecific Synthesis of the Chain Compound Senecivernic Acid. -A highly efficient synthesis of senecivernic acid (XV), a metabolite of the pyrrolizidine alkaloid senecivernine,