Autor: |
Paul G. Gassman, David B. Gorman, David B. Rusterholz |
Jazyk: |
angličtina |
Rok vydání: |
1997 |
Předmět: |
|
Zdroj: |
Molecules, Vol 2, Iss 5, Pp 80-86 (1997) |
Druh dokumentu: |
article |
ISSN: |
1420-3049 |
DOI: |
10.3390/20500080 |
Popis: |
Two 1,3,8,10-undecatetraenes were synthesized to test the viability of the intramolecular radical cation induced Diels-Alder reaction in the diene - diene format. Cyclization was successful only for the substituted tetraene with the lower oxidation potential. The major hexahydroindene product possessed a trans ring juncture demonstrating a selectivity for the endo stereochemistry. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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