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Percy, J.M.1
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3
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Organo-Fluorine Compounds
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Thieme: Stuttgart Elegant new approaches that include the Claisen rearrangement, and electroreductive defluorination have appeared recently
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Baasner, B.; Hagemann, H.; Tatlow, J. C. Organo-Fluorine Compounds. In Houben-Weyl Methods of Organic Chemistry; Thieme: Stuttgart, 1999; Vol. E 10a. Elegant new approaches that include the Claisen rearrangement, and electroreductive defluorination have appeared recently.
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Tatlow, J.C.3
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Uneyama, K.1
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0032565943
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Ishihara, T.; Takahashi, A.; Hayashi, H.; Yamanaka, H.; Kubota, T. Tetrahedron Lett. 1998, 39, 4691-4694.
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Ishihara, T.1
Takahashi, A.2
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Yamanaka, H.4
Kubota, T.5
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8
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0033615715
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Shibuya, S.5
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1842663065
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0001387472
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Burton and Yang have reported the synthesis of α,α-difluorohomoallylic alcohols by gem-difluoroallylation of aldehydes and ketones via the in situ reaction of 3-bromo-3,3-difluoropropene with acid-washed zinc powder:
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Burton and Yang have reported the synthesis of α,α-difluorohomoallylic alcohols by gem-difluoroallylation of aldehydes and ketones via the in situ reaction of 3-bromo-3,3-difluoropropene with acid-washed zinc powder: Yang, Z.-Y.; Burton, D. J. J. Org. Chem. 1991, 56, 1037-1041.
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0042869554
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Rücker, C.1
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17
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0343665781
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2O: C, 68.13; H, 9.64. Found: C, 68.08; H, 9.74.
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2O: C, 68.13; H, 9.64. Found: C, 68.08; H, 9.74.
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-
-
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18
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-
0342795549
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+-43, 3), 253 (4), 203 (3), 169 (8), 131 (4), 105 (20), 85 (100).
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+-43, 3), 253 (4), 203 (3), 169 (8), 131 (4), 105 (20), 85 (100).
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