and Regioselective Ni-Catalyzed Homoallylation of Aldimines with

Jun 23, 2005 - Masanari Kimura, Atsuko Miyachi,. Keisuke Kojima, Shuji Tanaka, and Yoshinao Tamaru*. Page 14361. Table 2, run 5. The structure 2k has ...
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Biomimetic Studies on Anti-Thyroid Drugs and Thyroid Hormone Synthesis [J. Am. Chem. Soc. 2004, 126, 2712-2713]. Gouriprasanna Roy, Munirathinam Nethaji, and G. Mugesh* Page 2712. The structure of compound 7 was incorrect. The correct structure is shown below:

Supporting Information, page 3. The concentration of H2O2 used for the LPO assay was 28.67 µM and not 287 nM as mentioned. JA053245Q 10.1021/ja053245q Published on Web 06/23/2005

Highly Stereo- and Regioselective Ni-Catalyzed Homoallylation of Aldimines with Conjugated Dienes Promoted by Diethylzinc [J. Am. Chem. Soc. 2004, 126, 14360-14361]. Masanari Kimura, Atsuko Miyachi, Keisuke Kojima, Shuji Tanaka, and Yoshinao Tamaru* Page 14361. Table 2, run 5. The structure 2k has been established as 2k′ by X-ray crystallography. The points that should be noted are (1) the reaction is 1,2-anti-selective and (2) cyclohexadiene shows different reactivity than other dienes and allylation, not homoallylation, takes place selectively.

JA0599115 10.1021/ja0599115 Published on Web 06/21/2005

10.1021/ja053245q CCC: $30.25 © 2005 American Chemical Society

J. AM. CHEM. SOC. 2005, 127, 10117

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