Catalytic Enantioselective Hetero-Diels−Alder Reactions of an Azo

Míriam Álvarez-Corral , Manuel Muñoz-Dorado and Ignacio Rodríguez-García. Chemical Reviews 2008 108 (8), 3174-3198. Abstract | Full Text HTML | P...
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Catalytic Enantioselective Hetero-Diels-Alder Reactions of an Azo Compound [J. Am. Chem. Soc. 2006, 128, 16482-16483]. Masanori Kawasaki and Hisashi Yamamoto* Supporting Information, pp S1-S2. The description of the preparation of azopyridine was incorrect. The corrected version is now available. Supporting Information Available: Corrected preparation of azopyridine. This material is available free of charge via the Internet at http://pubs.acs.org. JA076887H 10.1021/ja076887h Published on Web 04/07/2007

Highly Active, Stable, and Selective Well-Defined Silica Supported Mo Imido Olefin Metathesis Catalysts [J. Am. Chem. Soc. 2007, 129, 1044-1045]. Fre´ de´ ric Blanc, Jean Thivolle-Cazat, Jean-Marie Basset, Christophe Cope´ ret,* Adam S. Hock, Zachary J. Tonzetich, Amritanshu Sinha, and Richard R. Schrock* Page 1044. Amritanshu Sinha (affiliated with Massachusetts Institute of Technology) was inadvertently omitted from the author list in the published paper. The author list should read as follows: Fre´de´ric Blanc,‡ Jean Thivolle-Cazat,‡ Jean-Marie Basset,‡ Christophe Cope´ret,*,‡ Adam S. Hock,† Zachary J. Tonzetich,† Amritanshu Sinha,† and Richard R. Schrock*,†

Crystal Nucleation, Growth, and Morphology of the Synthetic Malaria Pigment β-Hematin and the Effect Thereon by Quinoline Additives: The Malaria Pigment as a Target of Various Antimalarial Drugs [J. Am. Chem. Soc. 2007, 129, 2615-2627]. Inna Solomonov,† Maria Osipova,† Yishay Feldman,‡ Carsten Baehtz,§ Kristian Kjaer,| Ian K. Robinson,⊥ Grant T. Webster,# Don McNaughton,# Bayden R. Wood,# Isabelle Weissbuch,*,† and Leslie Leiserowitz*,† Page 2626. The second sentence of the last paragraph in the section, Model of Quinoline Binding to the Crystal Faces of β-Hematin, “During this process a quinoline molecule may also bind to a β-hematin molecular dimer before the latter is adsorbed on a crystal surface, as proposed by Sullivan and Chong,29 but which has a kinetic disadvantage...”, is to be replaced by the following: During this process a quinoline molecule may also bind to a free heme (monomer or dimer), as proposed by O’Neill et al. (O’Neill, P. M.; Willock, D. J.; Hawley, S. R.; Bray, P. B.; Storr, R. C.; Ward, S. A.; Park, B. K. J. Med. Chem. 1997, 40, 437-448) and Sullivan and Chong,29 before a drug-heme complex may be adsorbed onto the crystal surface. However, in the event of such a quinoline-dimer complexation, it would incur a kinetic disadvantage... JA076888+ 10.1021/ja076888+ Published on Web 04/07/2007

JA071561U 10.1021/ja071561u Published on Web 04/06/2007

10.1021/ja076887h CCC: $37.00 © 2007 American Chemical Society

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