Phenyliodine diacetate-mediated oxidative cleavage of cyclobutanols leading to γ-hydroxy ketones
H Fujioka, H Komatsu, A Miyoshi, K Murai, Y Kita
Index: Fujioka, Hiromichi; Komatsu, Hideyuki; Miyoshi, Akihito; Murai, Kenichi; Kita, Yasuyuki Tetrahedron Letters, 2011 , vol. 52, # 9 p. 973 - 975
Full Text: HTML
Citation Number: 9
Abstract
Hypervalent iodine reagents are widely recognized as low-toxic oxidizing agents for use in the place of highly toxic heavy metal oxidizing reagents and many oxidation methods have been developed. 1 We have also been developing many synthetic reactions using the hypervalent iodine reagents. 2 We recently reported the reaction of phenol compounds with benzylic tert-cyclobutanols and phenyliodine diacetate (PIDA) to afford spiro cyclohexadienone ...
Related Articles:
[Matano, Yoshihiro; Nomura, Hazumi Angewandte Chemie - International Edition, 2002 , vol. 41, # 16 p. 3028 - 3031]
[Echavarren, Antonio M.; Perez, Marta; Castano, Ana M.; Cuerva, Juan M. Journal of Organic Chemistry, 1994 , vol. 59, # 15 p. 4179 - 4185]
[Fuji; Usami; Kiryu; Node Synthesis, 1992 , # 9 p. 852 - 858]
[Abe, Manabu; Inakazu, Tomoyasu; Munakata, Johichi; Nojima, Masatomo Journal of the American Chemical Society, 1999 , vol. 121, # 28 p. 6556 - 6562]
[Yang, Shao-Bo; Gan, Feng-Feng; Chen, Guo-Ju; Xu, Peng-Fei Synlett, 2008 , # 16 p. 2532 - 2534]