Concept
A Shift in Retrosynthetic Paradigm
Article first published online: 18 JUN 2008
DOI: 10.1002/chem.200800580
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Marek, I. (2008), A Shift in Retrosynthetic Paradigm. Chem. Eur. J., 14: 7460–7468. doi: 10.1002/chem.200800580
Publication History
- Issue published online: 25 AUG 2008
- Article first published online: 18 JUN 2008
Funded by
- Israel Science Foundation administrated by the Israel Academy of Sciences and Humanities. Grant Number: 459/04
- German-Israeli Foundation for Scientific Research and Development. Grant Number: GIF Research Grant No. I-871-62.5/2005
- United States–Israel Binational Science Foundation. Grant Number: 2005128
- Technion Research & Development
- Abstract
- Article
- References
- Cited By
Keywords:
- allylation;
- carbometalation;
- synthetic methods;
- zinc carbenoids
Abstract
The current state-of-the-art synthesis for the formation of enantiomerically enriched all-carbon quaternary stereocenters in acyclic system relies on the formation of a single carbon
carbon bond per chemical step by asymmetric catalysis. These extraordinary sophisticated methods were logically classified among the most powerful and innovative ones. In this concept article, we are proposing a new retrosynthetic paradigm to solve differently such challenging problems. These new synthetic pathways lead to the diastereo- and enantiomerically pure formation of three new carbon
carbon bonds in acyclic system, in a one-pot reaction, including the formation of all-carbon quaternary stereocenters by using classical reagents and experimental conditions and from common starting materials.

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