Thomas J. J. Müller of the Universität Heidelberg has reported (Chem. Methyltrioxorhenium(VII) structure 5-(Thiazol-5-yl)nicotinic acid web Commun. 2005, 2581.DOI: 10.1039/b502324f)a powerful method for the assembly of highly substituted furans, Pd-mediated…
Enantiomerically-pure carbocycles can be prepared either de novo, or by desymmetrization of prochiral rings. A classic illustration of the latter approach is the condensation of cyclohexanone (1) with p-nitrobenzaldehyde (2).…
The Strecker synthesis is the one-carbon homologation of an aldehyde to the α-amino nitrile. Robert Cunico of Northern Illinois University in DeKalb reports (Tetrahedron Lett. 2003, 44, 8025.DOI: 10.1016/j.tetlet.2003.09.006)a modified…
Homoallylic secondary alcohols such as 1 are readily prepared in enantiomerically-pure form by enantioselective addition of allyl anions to the aldehyde. Subhas Chandra Roy of the Indian Association for the…
Keiji Maruoka of Kyoto University has developed highly selective catalysts for the alkylation of protected glycine anions. PMID:23600560 He has now shown (J. Am. Chem. Soc. 2005, 127, 5073.DOI: 10.1021/ja0459328)that…
Aryl amines are common constituents of pharmaceuticals, so there has been a great deal of interest in their preparation, e.g by Pd- or Cu-mediated amination of aryl halides. Multi-step procedures…
Alkene metathesis (“Grubbs Reaction”) is now well-developed as a synthetic method. Still, there is a continuing effort to develop more efficient catalysts, and to extend the range of substrates that…
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