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Intramolecular Heck Reaction for the Synthesis of Isochromanes under Ambient and High pressure

โœ 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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โœฆ Synopsis


Abstract

The iodoarenes 9 and 10, bearing (E)โ€ and (Z)โ€alkene moieties, respectively, easily prepared by alkylation of the corresponding alcohols 7aโ€“c and 8aโ€“c with 2 iodobenzyl iodide, undergo intramolecular Heck reactions to give the isochromanes 12โ€“15aโ€“c 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. Highโ€pressure 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.


๐Ÿ“œ SIMILAR VOLUMES


Diastereo- and Regioselective Intramolec
โœ Tietze, Lutz F. ;Burkhardt, Olaf ;Henrich, Marielouise ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 751 KB

## Abstract Alkylation and acylation of the alkenes 9b, c and 10a, b, which are easily prepared from the corresponding ฮฑโ€amino alcohols, with 2โ€halobenzyl and 2โ€halobenzoyl halides respectively, gives 11โ€“15. These compounds cyclize with excellent diastereoโ€ and regioselectivity to the enantiomerica