Diastereoselective Cyclocondensation of Electron-Rich Dienes with Chiral Thio-Substituted Aldehydes

DOI: 10.1021/jo00039a019

Source and publish data:

Journal of Organic Chemistry p. 3605 - 3609 (1992)

Update date:2022-08-05

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Authors:

Annunziata, Rita

Cinquini, Mauro

Cozzi, Franco

Cozzi, Giorgio Pier

Raimondi, Laura

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Article abstract of DOI:10.1021/jo00039a019

The Lewis acid-promoted cyclocondensation between two electron-rich dienes with a series of racemic α- and β-thio-substituted aldehydes has been studied.Boron trifluoride etherate proved to be the catalyst of choice, affording satisfactory chemical yields

Full text of DOI:10.1021/jo00039a019

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