Correction to Aldol Condensation of Evans Chiral Enolates with

Jan 20, 2011 - Kitson, R. R. A.; Perry, A.; Scott, M. S.; Whitwood, A. C.;. Taylor, R. J. K.Eur. J. Org. Chem.2008, 4769-4783. (b) Lewis,. F. D.; Oxma...
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Correction to Aldol Condensation of Evans Chiral Enolates with Acetophenones. Its Application to the Stereoselective Synthesis of Homochiral Antifungal Agents [J. Org. Chem. 1995, 60, 3000. DOI: 10.1021/jo00115a014]. Javier Bartroli,* Enric Turmo, Jordi Belloc, and Javier Forn Page 3002. In this paper we inadvertently reversed six numerical values for compounds that we correct here. In Table 1, in the column “halohydrins”, where it reads A1(8) it should read A1(9), and where it reads A2(9) it should read A2(8). Page 3003. In the same way, in Table 2, in the column “epoxides”, where it reads A1(12) it should read A1(13), and where it reads A2(13) it should read A2(12). Page 3010. In the last paragraph of this page, where it reads syn-(2R,3R) (6a) it should read syn-(2R,3R) (7a), and where it reads syn-(2S,3S) (7a) it should read syn-(2S,3S) (6a). DOI: 10.1021/jo1024909 Published on Web 01/20/2011

Correction to Diastereoselective Synthesis of (( ()-Heliotropamide by a One-Pot, Four-Component Reaction [J. Org. Chem. 2010, 75, 8333. DOI: 10.1021/jo1019317]. Ashkaan Younai, Gregory F. Chin, and Jared T. Shaw* Page 8333. Although the spectroscopic and crystallographic data for compound 20 were attributed to Taylor, the accompanying citation was inadvertently omitted. The sentence should read as follows: “The close chemical shifts of heliotropamide and bisavenanthramide B to each other and to the related lactone 20 reported by Taylor,10a for which there is an accompanying X-ray crystal structure, support the assignment of heliotropamide as E.” Reference 10 should appear as follows: (10) The 1H NMR shifts of the vinylic proton in related alkylidene γ-lactams and lactones is generally 0.4-0.6 ppm higher upfield for the Z isomer when compared to the E isomer. See: (a) Edwards, M. G.; Kenworthy, M. N.; Kitson, R. R. A.; Perry, A.; Scott, M. S.; Whitwood, A. C.; Taylor, R. J. K. Eur. J. Org. Chem. 2008, 4769-4783. (b) Lewis, F. D.; Oxman, J. D.; Gibson, L. L.; Hampsch, H. L.; Quillen, S. L. J. Am. Chem. Soc. 1986, 108, 3005-3015. (c) Ezquerra, J.; Pedregal, C.; Yruretagoyena, B.; Rubio, A.; Carreno, M. C.; Escribano, A.; Ruano, J. L. G. J. Org. Chem. 1995, 60, 2925-2930. (d) Kang, J.-H. C.; H.-E.; Kim, S. Y.; Kim, Y.; Lee, J.; Lewin, N. E.; Pearce, L. V.; Blumberg, P. B.; Marquez, V. E. Bioorg. Med. Chem. 2003, 11, 2529-2539. (e) Cohen, J. L.; Chamberlin, A. R. J. Org. Chem. 2007, 72, 9240-9247. DOI: 10.1021/jo102536d Published on Web 01/20/2011

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