Issue 10 of OBC
01 May 2008
In this issue's Emerging Area, also a hot article, Yoshiki Morimoto (Osaka City University, Japan) reports the total assignments of the previously incomplete stereostructures of three members of the oxasqualenoids, through the first asymmetric total syntheses of the natural products.
The Perspective, by Wen-Xiong Zhang and Zhaomin Hou (RIKEN, Japan), shows how the addition of alkyne C-H, amine N-H and phosphine P-H bonds to carbodiimides can provide an efficient route to propiolamidines, guanidines, and phosphaguanidines. This work is also features on the inside front cover.
The outside front cover is supplied by Veronique Gouverneur (University of Oxford, UK) whose communication reports the synthesis of enantioenriched propargylic fluorides from enantioenriched allenylsilanes.
The Perspective, by Wen-Xiong Zhang and Zhaomin Hou (RIKEN, Japan), shows how the addition of alkyne C-H, amine N-H and phosphine P-H bonds to carbodiimides can provide an efficient route to propiolamidines, guanidines, and phosphaguanidines. This work is also features on the inside front cover.

The outside front cover is supplied by Veronique Gouverneur (University of Oxford, UK) whose communication reports the synthesis of enantioenriched propargylic fluorides from enantioenriched allenylsilanes.

References
Yoshiki Morimoto, Org. Biomol. Chem., 2008, DOI: 10.1039/b801126e
Wen-Xiong Zhang and Zhaomin Hou, Org. Biomol. Chem., 2008, DOI: 10.1039/b800135a
Laurence Carroll, Samantha McCullough, Tom Rees, Timothy D. W. Claridge and Véronique Gouverneur, Org. Biomol. Chem., 2008, DOI: 10.1039/b803888k
Organic & Biomolecular Chemistry Issue 10
View the contents of this issue
Short personal accounts of a new area of research.
Easy-to-read articles covering current areas of interest.
