## Abstract The reaction between an α,β‐unsaturated pyruvate and ethyl diazoacetate (EDA) yielded two unexpected products. The structures of these products were determined by automated elucidation of the chemical structures using spectroscopic inputs of a series of 1D and 2D NMR data using the comp
Structure elucidation of an unexpected product from dehydration of a β-hydroxyketone
✍ Scribed by David E. Minter; Christopher D. Winslow; William H. Watson; Satish Bodige
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 162 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1873
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✦ Synopsis
Abstract
The structure of an unexpected compound from the dehydration of an aldol addition product has been determined using 1‐D and 2‐D NMR techniques. This reaction is the last step in a new synthetic approach to the galanthan ring system. Complete ^1^H and ^13^C NMR assignments for two synthetic precursors are also reported. Copyright © 2006 John Wiley & Sons, Ltd.
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