Synthesis and Reactivity of Bicycles Derived from Tartaric Acid and

Bicycles Derived from Tartaric Acid and R-Amino Acids: A Novel. Class of Conformationally Constrained Dipeptide Isosteres Based upon Enantiopure 3-Aza...
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J. Org. Chem. 2000, 65, 4782

Additions and Corrections Vol. 64, 1999 Anna Cappa, Enrico Marcantoni,* Elisabetta Torregiani, Giuseppe Bartioli, Maria Cristina Bellucci, Marcella Bosco, and Letizia Sambri. A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide.

Page 5696, right column, line 7. The following sentence should have been added after the period: “The use of iodine in methanol is a simple and mild method for the selective deprotection of p-methoxybenzyl ethers. (Vaino, A. R.; Szarek, W. A. Synlett 1995, 1157-1158.)” We have inadvertently omitted this paper in our reference citations. JO0040238 10.1021/jo0040238 Published on Web 06/27/2000

Antonio Guarna,* Antonio Guidi, Fabrizio Machetti, Gloria Menchi, Ernesto G. Occhiato, Dina Scarpi, Sauro Sisi, and Andrea Trabocch. Synthesis and Reactivity of Bicycles Derived from Tartaric Acid and R-Amino Acids: A Novel Class of Conformationally Constrained Dipeptide Isosteres Based upon Enantiopure 3-Aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylic Acid.

Page 7358. 1H NMR data for compound 60 should read: δ 9.32 (s, 1 H), 7.40-7.00 (m, 10 H), 5.34 (d, J ) 5.8 Hz, 1 H), 4.95 (d, J ) 5.8 Hz, 1 H), 4.90 (d, J ) 15.4 Hz, 1 H), 3.86 (s, 3 H), 3.51 (dd, J ) 8.3, 4.4 Hz, 1 H), 3.36 (dd, J ) 13.9, 4.4 Hz, 1 H), 3.19 (d, J ) 15.4 Hz, 1 H), 3.16 (dd, J ) 13.9, 8.3 Hz, 1 H), 1.49 (s, 3 H), 1.43 (s, 3 H). JO004022F 10.1021/jo004022f Published on Web 06/29/2000

Vol. 65, 2000 John Dogan, Jurgen B. Schulte, Gerhard F. Swigers,* and S. Bruce Wild. Mechanism of Phosphorus-Carbon Bond Cleavage in Tertiary Phosphines. An Optimized Synthesis of 1,2Bis(phenylphosphino)ethane.

Page 952: Equation 1 should read Li

R′R′′R′′′P 98 R′R′′R′′′P•- Li+ f R′R′′P- Li+ + Li

R′′′• 98 R′R′′P- Li+ + R′′′- Li+ (1) JO0040285 10.1021/jo0040285 Published on Web 06/27/2000