Acceleration of a Diels-Alder reaction in an ultracentrifuge
โ Scribed by Daniel P. Dolata; Rolf Bergman
- Book ID
- 104227448
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 120 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The presence of biphenylenediol8 accelerates the rate of some Die&Alder reactions. Catalysis via a complex involving two hydrogen bona5 (see 6) is proposed. The development of catalysts for the asymmetric induction of Diels-Alder reactions is a subject of considerable current interest. To date, att
The formation of two hydrogen bonds between an amidopyridine and a carboxylic acid controls the stereochemical outcome and significantly accelerates the rate of the Diels-Alder cycloaddition between a benzoylpyrrole and a maleimide.
Rapid and stereoselective Diels-Alder reactions can be run in ethanol or methy- lene chloride in the presence of FelI1-doped K10 montmorillonite. ## IMPRESSIVE improvements of the Diels-Alder reaction have been achieved recently.