Intramolecular Heck Reaction for the Synthesis of Isochromanes under Ambient and High pressure
โ Scribed by Tietze, Lutz F. ;Burkhardt, Olaf ;Henrich, Marielouise
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 535 KB
- Volume
- 1997
- Category
- Article
- ISSN
- 0947-3440
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โฆ Synopsis
Abstract
The iodoarenes 9 and 10, bearing (E)โ and (Z)โalkene moieties, respectively, easily prepared by alkylation of the corresponding alcohols 7aโc and 8aโc with 2 iodobenzyl iodide, undergo intramolecular Heck reactions to give the isochromanes 12โ15aโc in good yields. The selectivity of the reaction depends on the size of the substituent R in 9 and 10; increasing bulkiness of R leads to a decrease in diastereoselectivity and an increase in regioselectivity. Highโpressure experiments confirm the proposed mechanism and show that bromoarenes such as 11, which tend to be unreactive at ambient pressure, give good results when the cyclisation is performed under high pressure.
๐ SIMILAR VOLUMES
## Abstract Alkylation and acylation of the alkenes 9b, c and 10a, b, which are easily prepared from the corresponding ฮฑโamino alcohols, with 2โhalobenzyl and 2โhalobenzoyl halides respectively, gives 11โ15. These compounds cyclize with excellent diastereoโ and regioselectivity to the enantiomerica