Issue 19 of OBC
18 September 2008
In this issue's Emerging Area, David Carbery (University of Bath, UK) discusses recent applications of enamides in organic synthesis, substrates whose combination of reactivity and stability makes them very attractive to the synthetic community.
The work featured on the outside front cover (above), by Ka Wai Choi and Margaret Brimble (University of Auckland, New Zealand), describes a synthetic study to incorporate a triazole unit as a peptide bond surrogate into a spiroacetal derivative.
The issue's inside front cover (above) is provided by Ben Feringa and colleagues (University of Groningen, The Netherlands). The communication, which is also a hot article, presents a mild and rapid variation on the classical click reaction of azides and alkynes.

The work featured on the outside front cover (above), by Ka Wai Choi and Margaret Brimble (University of Auckland, New Zealand), describes a synthetic study to incorporate a triazole unit as a peptide bond surrogate into a spiroacetal derivative.

The issue's inside front cover (above) is provided by Ben Feringa and colleagues (University of Groningen, The Netherlands). The communication, which is also a hot article, presents a mild and rapid variation on the classical click reaction of azides and alkynes.
References
David R. Carbery, Org. Biomol. Chem., 2008, DOI: 10.1039/b809319a
Ka Wai Choi and Margaret A. Brimble, Org. Biomol. Chem., 2008, DOI: 10.1039/b808454h
Lachlan Campbell-Verduyn, Philip H. Elsinga, Leila Mirfeizi, Rudi A. Dierckx and Ben L. Feringa, Org. Biomol. Chem., 2008, DOI: 10.1039/b812403e
Organic & Biomolecular Chemistry Issue 19
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