Diels-alder reactions of 5,8-quinolineclione
✍ Scribed by Jal F. Munshi; Madeleine M. Joullié
- Book ID
- 112121562
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1967
- Tongue
- English
- Weight
- 295 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0022-152X
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📜 SIMILAR VOLUMES
The frontier molecular orbital of 5-phenylcyclopentadiene was predicted on the basis of the orbital mixing rule to deform to favor the Diels-Alder reaction in a syn contrasteric manner. The prediction was substantiated experimentally by the reactions of 5-methyl-5phenylcyclopentadiene with dienophil
IYiels-Alder reactions of 2,5,8(1If)quinoliaet were completely rcgiosekcuve for au the unsymmetrical &llert&e&uceptinthecaseofisopfaKlIliscmtspondstoa levelofregtosdectivity hi\*tban theefoundhybyviauwo&xforSSquindinecplinm. A number of studies are available on the regioselectivity of the Diels-Alde