𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Substituent effects on the orientation of Diels-Alder reactions. I

✍ Scribed by Schmidt, Cirill.


Book ID
118745119
Publisher
American Chemical Society
Year
1970
Tongue
English
Weight
718 KB
Volume
35
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Simple prediction of cycloaddition orien
✍ O. Eisentein; J.M. Lefour; NguyΓͺn Trong Anh; R.F. Hudson πŸ“‚ Article πŸ“… 1977 πŸ› Elsevier Science 🌐 French βš– 637 KB

Application of the "hard and soft" concept to the Woodward-Katz model allows simple and accurate prediction of the structure of the major adduct in Diels-Alder reactions. About 100 examples have been examined. Agreement with experimental results is excellent: therefore, the doubts expressed by Houk

Intramolecular diels-alder reactions of
✍ Daniel D. Sternbach; Debby M. Rossana πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 262 KB

An internal Diels-Alder reaction, using furan as the diene component, formed a highly functionalized 5-membered carbocycllc ring in excellent yield. Solvent and substituent effects of this reaction were examined. In connection with a proJect devoted to the synthesis of some natural products contai