[1] Hartmann C, Gattermann L. Ueber die verseifung von phenoläthern und derivaten derselben, sowie von s ure thern durch aluminiumchlorid[J]. Eur J Inorg Chem, 1892, 25(2): 3531-3534.
[2] Sagrera G, Seoane G. Acidic rearrangement of (benzyloxy)chalcones: a short synthesis of chamanetin[J]. Synthesis, 2009, 24: 4190-4202.
[3] Petchmanee T, Ploypradith P, Ruchirawat S, et al. Solid-supported acids for debenzylation of aryl benzyl ethers[J]. J Org Chem, 2006, 71(7): 2892-2895.
[4] Bhure MH, Rode CV, Chikate RC, et al. Phosphotungstic acid as effcient solid catalyst for intramolecular rearrangement of benzyl phenyl ether to 2-benzyl phenol[J]. Catal Commun, 2007, 8: 139-144.
[5] Rode CV, Garade AC, Chikate RC. Solid acid catalysts: modification of acid sites and effect on activity and selectivity tuning in various reactions[J]. Catal Surv Asia, 2009,13:205-220.
[6] Khabnadideh S, Pez D, Musso A, et al. Design, synthesis and evaluation of 2,4-diaminoquinazolines as inhibitors of trypanosomal and leishmanial dihydrofolate reductase[J]. Bioorg Med Chem, 2005, 13(7): 2637-2649.
[7] Pitchumani K, Devanathan S, Ramamurthy V. Modification of photochemical reactivity on formation of inclusion complexes: photorearrangement of benzyl phenyl ethers and methyl phenoxyacetates[J]. J Photochem Photobiol A:Chem, 1992, 69: 201-208.
[8] Ramamurthy V. Organic photochemistry in organized media[J]. Tetrahedron, 1986, 42(21): 5753-5839.
[9] Kelly DP, Pinhey JT. The photochemical rearrangement of phenoxyacetic acids[J]. Tetrahedron Lett, 1964, 46(5): 3427-3429.
[10] Ozawa S, Suenaga T, Ogino Y. Effects of molten tin surface upon the reaction of benzyl phenyl ether[J]. Fuel, 1985, 64(5): 712-714.
[11] Shimamura N, Sugimori A. Direct and sensitized photoreactions of allyl phenyl ether[J]. Bull Chem Soc Jpn, 1971, 44(1): 281-283.
[12] Xu JQ, George M, Weiss RG. Photo-fries rearrangements of 1-naphthyl (R)-2-phenylpropanoate in poly(vinyl acetate) and ethyl acetate. Influence of medium polarity and polymer relaxation on motions of singlet radical pairs[J]. Ann Braz Acad Sci, 2006, 78(1): 31-44.
[13] Tarbell DS,Petropoulos JC. The action of aluminum bromide on benzyl phenyl ether[J]. J Am Chem Soc, 1952, 74(5): 244-248.
[14] Hart H, Eleuterio HS . The stereochemistry of aromatic alkylations II. the thermal rearrangement of alkyl aryl ethers[J]. J Am Chem Soc, 1954, 76(2): 519-522.
[15] Hart LS, Waddington CR. Aromatic rearrangements in the benzene series. Part 4. intramolecularity of both the ortho- and para-rearrangements of benzyl phenyl ether as shown by labelling experiments[J]. J Chem Soc, 1985,Perkin Trans II:1607-1612.
[16] Hart H,Kosak JR. Stereochemical control by solvent in the thermal rearrangement of aryl α-phenethyl ethers[J]. J Org Chem, 1958, 23: 2019-2020.
[17] Dewar MJS, Pierini AB. Mechanism of the diels-alder reaction. Studies of the addition of maleic anhydride to furan and methylfurans[J]. J Am Chem Soc, 1984, 106(1): 203-208.