Synthesis of acid-resistant p-quinone monoketals and thermally stable 4,4-dialkoxycyclohexa-2,5-dien-1-ols

Article abstract of DOI:10.1080/00397910008087100

Preparation and high resistance to acid hydrolysis of sterically hindered p-quinone monoketals 1a, 1b and 1c are described. Thermal stability of ketal alcohols 2a and 2b derived from 1a and 1c, respectively, is also mentioned.

Full text of DOI:10.1080/00397910008087100

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
Synthesis of Acid-Resistant P-Quinone Monoketals
and Thermally Stable 4,4-Dialkoxycyclohexa-2,5-
Dien-1-OLS
Kanji Omura
To cite this article: Kanji Omura (2000) Synthesis of Acid-Resistant P-Quinone Monoketals
and Thermally Stable 4,4-Dialkoxycyclohexa-2,5-Dien-1-OLS, Synthetic Communications, 30:5,
877-885, DOI: 10.1080/00397910008087100
To link to this article: http://dx.doi.org/10.1080/00397910008087100
Published online: 04 Dec 2007.
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Date: 06 March 2016, At: 21:19