Preparation of the 8, 9-epoxide of the mycotoxin aflatoxin B1: the ultimate carcinogenic species
SW Baertschi, KD Raney, MP Stone…
Index: Baertschi; Raney; Stone; Harris Journal of the American Chemical Society, 1988 , vol. 110, # 23 p. 7929 - 7931
Full Text: HTML
Citation Number: 224
Abstract
Q In 3 n-1 4 n-2 was complete within 15 min at room temperature giving the epoxide and acetone as the only products. The present procedure avoids the presence of electrophiles or nucleophiles. Solvent and excess dimethyldioxirane were removed by evaporation in a stream of nitrogen to leave 2 as a. solid which could be recrystallized from acetone and methylene ch10ride. I~ The crystalline material underwent a phase transition near 230 OC ...
Related Articles:
[Gopalakrishnan, S.; Stone, Michael P.; Harris, Thomas M. Journal of the American Chemical Society, 1989 , vol. 111, # 18 p. 7232 - 7239]
[Pelkonen; Lang; Negishi; Wild; Juvonen Chemical research in toxicology, 1997 , vol. 10, # 1 p. 85 - 90]