Facile Preparation of Doubly Dipyrrolylquinoxaline-Bridged Expanded

Florence Szydlo, Bruno Andrioletti*, and Eric Rose. Org. Lett. , 2006, 8 (21), pp 4983–4983. DOI: 10.1021/ol062146u. Publication Date (Web): Septemb...
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ORGANIC LETTERS 2006 Vol. 8, No. 21 4983

Additions and Corrections

Volume 4, 2002

Teck-Peng Loh,* Hong-Yan Song, and Yan Zhou Nickel-Catalyzed Homoallylation Reaction of Aldehydes with 1,3-Dienes: Stereochemical and Mechanistic Studies. Page 2716, Table 1, entry 5, and page 2717, Table 2. We reported that a bishomoallylic alcohol was obtained while using 1,3-cyclohexadiene. However, we learned that the structures of compounds 9 and 12 were incorrectly assigned. Compounds 9 and 12a-e should be homoallylic alcohols. In this reaction, cyclohexadiene shows different reactivity than other dienes, and allylation takes place selectively.1 We thank Professor Yoshinao Tamaru for calling our attention to this error. (1) (a) Kimura, M.; Miyachi, A.; Kojima, K.; Tanaka, S.; Tamaru, Y. J. Am. Chem. Soc. 2005, 127, 10117. (b) Kimura, M.; Ezoe, A.; Mori, M.; Iwata, K.; Tamaru, Y. J. Am. Chem. Soc. 2006, 128, 8559.

OL062226Y 10.1021/ol062226y Published on Web 09/16/2006

Volume 8, 2006

Florence Szydlo, Bruno Andrioletti,* and Eric Rose Facile Preparation of Doubly Dipyrrolylquinoxaline-Bridged Expanded Porphyrins. Synthesis and Structural Characterization of an Unprecedented [20]Tetraphyrin-(2.1.2.1). Page 2345. The incorrect Supporting Information was submitted for this manuscript. This has now been replaced with the correct version. OL062146U 10.1021/ol062146u Published on Web 09/07/2006