Understanding the Torquoselectivity in 8π-Electrocyclic Cascade Reactions: Synthesis of Fenestradienes versus Cyclooctatrienes-Reference-Cited by-同舟云学术

Understanding the Torquoselectivity in 8π-Electrocyclic Cascade Reactions: Synthesis of Fenestradienes versus Cyclooctatrienes

Published:2009-08-28 Issue:37 Volume:131 Page:13387-13398
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hulot Catherine¹,Amiri Shadi¹,Blond Gaëlle¹,Schreiner Peter R.¹,Suffert Jean¹

Affiliation:

1. Faculté de Pharmacie, Université de Strasbourg (UMR 7200 CNRS/UDS), 74 Route du Rhin, 67401 Illkirch/Strasbourg, France, and Institut für Organische Chemie, Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 58, D-35392 Giessen, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja903914r

Reference89 articles.

1. Theory of stereoselection in conrotatory electrocyclic reactions of substituted cyclobutenes

2. Electrocyclic ring openings of dialkylcyclobutenes: anomalies explained

3. Prediction and experimental verification of the stereoselective electrocyclization of 3-formylcyclobutene

4. Transition structures of pericyclic reactions. Electron correlation and basis set effects on the transition structure and activation energy of the electrocyclization of cyclobutene to butadiene

5. Electrocyclic reactions of 1-substituted 1,3,5,7-octatetraenes. An ab initio molecular orbital study of torquoselectivity in eight-electron electrocyclizations

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