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Iodine-Initiated Domino Reaction of Hepta-1,2-dien-6-yn-4-ols and Brønsted Acid Promoted Cyclization of Hepta-1,2,6-trien-4-ols Leading to Functionalized Benzenes.
- Source :
- Chemistry - An Asian Journal; Apr2013, Vol. 8 Issue 4, p717-722, 6p
- Publication Year :
- 2013
-
Abstract
- Buy one get one free: Concurrent introduction of both iodo ‐ and carbonyl groups, along with the construction of the benzenoid core, has been achieved through an iodine ‐ initiated domino reaction of hepta ‐ 1,2 ‐ dien ‐ 6 ‐ yn ‐ 4 ‐ ols. Moreover, cyclization of hepta ‐ 1,2,6 ‐ trien ‐ 4 ‐ ols turns out to also be an efficient pathway toward diversely substituted benzenes. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 18614728
- Volume :
- 8
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- Chemistry - An Asian Journal
- Publication Type :
- Academic Journal
- Accession number :
- 86198205
- Full Text :
- https://doi.org/10.1002/asia.201201151