Cyclodimerization of α,β–α′,β′-unsaturated ketones promoted by samarium diiodide. Complete assignment of the 1H and 13C NMR spectra of hydroxycyclopentylpropenone derivatives
✍ Scribed by Ronan Le Lagadec; María Isabel Chávez; Laura Rubio; Armando Cabrera
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 130 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.823
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ^1^H and ^13^C NMR chemical shift assignments of hydroxycyclopentylpropenone derivatives, prepared by a highly selective reaction between samarium(II) iodide and unsaturated ketones, are described. Two‐dimensional shift‐correlated experiments (COSY, HMBC, HMQC, NOESY) were used to assign the chemical shifts completely and unambiguously. Copyright © 2001 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract The complete ^1^H and ^13^C chemical shift assignments of the 13α‐epimer of estrone methyl ether and of estrone methyl ether itself were carried out, making use of one‐ and two‐dimensional NMR techniques (1D HOHAHA, COSY, NOESY, TOCSY and HSQC). Copyright © 2001 John Wiley & Sons, Ltd.
## Abstract ^1^H and ^13^C NMR chemical shifts of α‐ and β‐anomers of adenosine, 2′‐deoxyadenosine and their acetate derivatives were completely and definitely assigned using the concerted application of one‐ and two‐dimensional experiments (gCOSY, gNOESY, gHSQC and gHMBC). The influence of the ste