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
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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 ...
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