Highly Regio- and Stereoselective Cyclic Iodoetherification of 4,5-Alkadienols. An Efficient Preparation of 2-(1′(Z)-Iodoalkenyl)tetrahydrofurans

In this paper, an efficient way to synthesize 2-(1′(Z)-iodoalkenyl)tetrahydrofurans from 4,5-alkadienols and I2 was developed. The reaction of the 4,5-allenols with a substituent in the 3-position afforded the trans-2,3-disubstituted tetrahydrofurans with very high diastereoselectivity. However, whe...

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Veröffentlicht in:Journal of organic chemistry 2009-01, Vol.74 (1), p.438-441
Hauptverfasser: Lü, Bo, Jiang, Xinpeng, Fu, Chunling, Ma, Shengming
Format: Artikel
Sprache:eng
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Zusammenfassung:In this paper, an efficient way to synthesize 2-(1′(Z)-iodoalkenyl)tetrahydrofurans from 4,5-alkadienols and I2 was developed. The reaction of the 4,5-allenols with a substituent in the 3-position afforded the trans-2,3-disubstituted tetrahydrofurans with very high diastereoselectivity. However, when the axially optically active 4,5-allenol was treated with I2 in n-hexane, the efficiency for chirality transfer was low. This problem was circumvented by conducting the reaction in CH2Cl2 at room temperature and applying N-iodosuccinimide as the electrophilic reagent; however, the Z/E ratio for the products is much lower. Highly optically active Z-products may be prepared via the kinetic resolution via a Sonogashira coupling reaction with propargyl alcohol.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo802079b