Rearrangements of Allylic Sulfinates to Sulfones: A Mechanistic Study-Reference-Cited by-同舟云学术

Rearrangements of Allylic Sulfinates to Sulfones: A Mechanistic Study

Published:2010-05-12 Issue:7 Volume:87 Page:717-720
ISSN:0021-9584
Container-title:Journal of Chemical Education
language:en
Short-container-title:J. Chem. Educ.

Author:

Ball David B.¹,Mollard Paul¹,Voigtritter Karl R.¹,Ball Jenelle L.²

Affiliation:

1. Department of Chemistry and Biochemistry, California State University, Chico, Chico, California 95929-0210

2. Chico High School, Chico, California 95926

Publisher

American Chemical Society (ACS)

Subject

Education,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ed100299x

Reference12 articles.

1. Saying What You Mean: Teaching Mechanisms in Organic Chemistry

2. aFor an excellent discussion of the theory pericyclic reactions seeAnslyn, E. V.; Dougherty, D. A.Modern Physical Organic Chemistry;University Science Books:Sausalito, CA, 2006; pp877−928.

3. The Aromaticity of Pericyclic Reaction Transition States

4. Computational Analysis of Stereospecificity in the Cope Rearrangement

5. Kinetic Derivations for Thermal Isomerizations of Monodeuterio Cyclic 1,3-Dienes through 1,5-Hydrogen Shifts

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