Azidolysis of α,β-Epoxycarboxylic Acids. A Water-Promoted Process Efficiently Catalyzed by Indium...
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Additions and Corrections Vol. 66, 2001 Francesco Fringuelli, Ferdinando Pizzo,* and Luigi Vaccaro. Azidolysis of R,-Epoxycarboxylic Acids. A Water- Promoted Process Efficiently Catalyzed by Indium Trichloride at pH 4.0 Page 3555, ref 20. There is an inversion of the pH values before and after addition of InCl 3 . The correct sentence is as follows: “The pH of a 2.5 M aqueous solution of NaN 3 (5 mol/equiv) containing the R,-epoxy- acid 4 (1 equiv) is 5.0 and becomes 4.5 in the presence (0.01 mol/equiv) of InCl 3 ...”. JO012954T 10.1021/jo012954t Published on Web 02/16/2002 Yasujiro Murata, Michihisa Murata, and Koichi Komatsu*. The Reaction of Fullerene C60 with 4,6-Dimethyl- 1,2,3-triazine: Formation of an Open-Cage Fullerene Derivative. Page 8190: In Figure 3, the structure number 8 and 21 should be interchanged. JO027960J 10.1021/jo027960j Published on Web 02/16/2002 1974 J. Org. Chem. 2002, 67, 1974
Transcript of Azidolysis of α,β-Epoxycarboxylic Acids. A Water-Promoted Process Efficiently Catalyzed by Indium...
Additions and Corrections
Vol. 66, 2001
Francesco Fringuelli, Ferdinando Pizzo,* and LuigiVaccaro. Azidolysis of R,â-Epoxycarboxylic Acids. A Water-Promoted Process Efficiently Catalyzed by Indium Trichlorideat pH 4.0
Page 3555, ref 20. There is an inversion of the pHvalues before and after addition of InCl3. The correctsentence is as follows: “The pH of a 2.5 M aqueoussolution of NaN3 (5 mol/equiv) containing the R,â-epoxy-acid 4 (1 equiv) is 5.0 and becomes 4.5 in the presence(0.01 mol/equiv) of InCl3...”.
JO012954T
10.1021/jo012954tPublished on Web 02/16/2002
Yasujiro Murata, Michihisa Murata, and KoichiKomatsu*. The Reaction of Fullerene C60 with 4,6-Dimethyl-1,2,3-triazine: Formation of an Open-Cage Fullerene Derivative.
Page 8190: In Figure 3, the structure number 8 and21 should be interchanged.
JO027960J
10.1021/jo027960jPublished on Web 02/16/2002
1974 J. Org. Chem. 2002, 67, 1974
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