Mechanism of Anionic [3 + 2] Cycloadditions. An ab Initio Computational Study on the Cycloaddition of Allyl-, 2-Borylallyl-, and 2-Azaallyllithium to Ethylene-Reference-Cited by-同舟云学术

Mechanism of Anionic [3 + 2] Cycloadditions. An ab Initio Computational Study on the Cycloaddition of Allyl-, 2-Borylallyl-, and 2-Azaallyllithium to Ethylene

Published:1998-03-31 Issue:14 Volume:120 Page:3357-3370
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Neumann Frank¹,Lambert Christoph¹,Schleyer Paul von Ragué¹

Affiliation:

1. Contribution from the Institut für Organische Chemie, Friedrich-Alexander Universität ErlangenNürnberg, Henkestrasse 42, D-91054 Erlangen, Germany, and Institut für Organische Chemie, Universität Regensburg, D-93040 Regensburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9735160

Reference100 articles.

1. Reaction of α-Methylstyrene Catalyzed by Sodium1

2. Potassium-Catalyzed Reactions of α-Methylstyrene with Alkylbenzenes1,2

3. Etude des reactions des reactifs de grignard allyliques vis a vis du benzyne et du cyclohexyne

4. Synthese fünfgliedriger Carbocyclen durch [1,3]-anionische Cycloaddition

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