Compared Behavior of 5-Deoxy-5-iodo-d-xylo- and l-Arabinofuranosides in the Reductive Elimination Reaction: A Strong Dependence on Structural Parameters and on the Presence of Zn2+. A Combined Experimental and Theoretical Investigation-Reference-Cited by-同舟云学术

Compared Behavior of 5-Deoxy-5-iodo-d-xylo- and l-Arabinofuranosides in the Reductive Elimination Reaction: A Strong Dependence on Structural Parameters and on the Presence of Zn2+. A Combined Experimental and Theoretical Investigation

Published:2007-03-01 Issue:7 Volume:72 Page:2271-2278
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Henon Eric¹,Bercier Ariane¹,Plantier-Royon Richard¹,Harakat Dominique¹,Portella Charles¹

Affiliation:

1. Groupe de Spectrométrie Moléculaire et Atmosphérique (GSMA), UMR CNRS 6089 and Réactions Sélectives et Applications (RSA), UMR CNRS 6519, U.F.R Sciences, Université de Reims Champagne-Ardenne, Moulin de la housse, B.P. 1039, 51687 Reims Cedex 2, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0614590

Reference37 articles.

1. Carbocyclische Verbindungen aus Monosacchariden. I. Umsetzungen in der glucosereihe

2. Substrate specificity and carbohydrate synthesis using transketolase

3. Novel synthesis of 5-thio-hexopyranoside: preparation of 5-thio-d- and l-glucose and 1,6-anhydro-5-thio-l- and d-altrose

4. Carbohydrate Carbocyclization by a Novel Zinc-Mediated Domino Reaction and Ring-Closing Olefin Metathesis

5. Ultrasound-accelerated synthesis of chiral allylic alcohols promoted by indium metal

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