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Studies related to biological detoxification of kraft pulp mill effluent. V. The synthesis of 12- and 14-chlorodehydroabietic acids and 12,14-dichlorodehydroabietic acid, fish-toxic diterpenes from kraft pulp mill effluent

✍ Scribed by James P. Kutney; Eugene Dimitriadis


Publisher
John Wiley and Sons
Year
1982
Tongue
German
Weight
416 KB
Volume
65
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

An improved synthesis of the isomeric 12‐ and 14‐chlorodehydroabietic acids (3 and 2, respectively) and 12,14‐dichlorodehydroabietic acid (4) is described. The monochioro isomers were conveniently separated as the imidazole derivatives, and conversion of the latter to the free acids or their corresponding methyl esters could be achieved in high yield. Studies involving microbial degradation of 2–4 are underway.


📜 SIMILAR VOLUMES


Studies Related to Biological Detoxifica
✍ James P. Kutney; Eugene Dimitriadis; Gary M. Hewitt; Philip J. Salisbury; Mahata 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 German ⚖ 452 KB

## Abstract A detailed study of the biodegradation of one of the fish toxic chlorinated resin acids, 12,14‐dichlorodehydroabietic acidThe correct IUPAC‐name is 12,14‐dichloro‐8,9,11,12‐tetradehydro‐7,8‐dihydroabietic acid. (**3**) is presented. When exposed to the fungus __Mortierella isabellina__

Studies Related to Biological Detoxifica
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## Abstract One of the fish‐toxic chlorinated resin acids, 14‐chlorodehydroabietic acid (**5**), found in kraft mill effluent is examined. When exposed to the fungus __Mortierella isabellina__, **5** is converted into a number of hydroxylated derivatives which show low levels of toxicity to fish. T

Studies related to biological detoxifica
✍ James P. Kutney; Gary M. Hewitt; Philip J. Salisbury; Mahatam Singh; James A. Se 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 German ⚖ 342 KB

## Abstract A detailed study of the biodegradation of one of the fish‐toxic chlorinated resin acids, 12‐chlorodehydroabietic acid **(3)**, is discussed. When **3** is exposed to the fungus __Mortierella isabellina__, it is converted into the monohydroxylated metabolites 2α‐hydroxy‐12‐chlorodehydroa