Coble A.B.'s A Proof of Whites Porism (1916)(en)(2s) PDF

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Hashhnoto S, Kameoka H. J Food Sc 1985; 50: 847-852. Lockwood GB, Afsharypuor S. J Chrom 1986; 356: 438-440. Bergstrom J, Bergstrom G. Nord J Bot 1989; 9: 363-366. Smith PA. Open-Chain Nitrogen Compounds Vol 1. New York: WA Benjamin Inc, 1965. Strobel GA. J Biol Chem 1966; 241: 2618-2621. Uematsu T, Suhadolnik RJ. Arch Biochem Biophys 1974; 162: 614-619. Ashton FM, Crafl~ AS. Mode of Action of Herbicides. New York: John Wiley & Sons Inc, 1973; 236-255. Henahan YF, Yames D, Idol Yr. Chem Eng News 1971; 49: 16-18.

Carbamic acid and N-substituted derivatives are unstable; they decompose spontaneously to carbon dioxide and ammonia or amine. Anilides are arylamides of carboxylic acids. For all these compounds, hydrolysis is the most important reaction involved in the biodegradation of ester or amide linkage (Figure 13) [196]. Ct A l Ct II N--C--C2Hs ~ ~ Propanil Clk):_~ B ~ H Cl~ Linuron C[ ~~,, C 0 CH I II / 3 N---C --N \ H 0 I II Ct C[__~NH2 J OCH3 CH3 i Ct N---C--O--CH I CH 3 Chlorpropham Figure 13. Hydrolysis of herbicides: A, phenylamide; B, phenylurea; C, phenylcarbamate [196].

Lockwood GB, Afsharypuor S. J Chrom 1986; 356: 438-440. Bergstrom J, Bergstrom G. Nord J Bot 1989; 9: 363-366. Smith PA. Open-Chain Nitrogen Compounds Vol 1. New York: WA Benjamin Inc, 1965. Strobel GA. J Biol Chem 1966; 241: 2618-2621. Uematsu T, Suhadolnik RJ. Arch Biochem Biophys 1974; 162: 614-619. Ashton FM, Crafl~ AS. Mode of Action of Herbicides. New York: John Wiley & Sons Inc, 1973; 236-255. Henahan YF, Yames D, Idol Yr. Chem Eng News 1971; 49: 16-18. Salame M, Nemphos SP. In: Proceedings of the Symposium on Environmental Impact of Nitrile Barrier Containers.

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