Volume 51, Issue 28 p. 6796
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Inside Cover: CH Activation in S-Alkenyl Sulfoximines: An Endo 1,5-Hydrogen Migration (Angew. Chem. Int. Ed. 28/2012)

Xuefeng Gao

Xuefeng Gao

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Vikram Gaddam

Vikram Gaddam

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Erich Altenhofer

Erich Altenhofer

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Rama Rao Tata

Rama Rao Tata

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Zhengxin Cai

Zhengxin Cai

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Nattawut Yongpruksa

Nattawut Yongpruksa

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Aswin K. Garimallaprabhakaran

Aswin K. Garimallaprabhakaran

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

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Prof. Michael Harmata

Corresponding Author

Prof. Michael Harmata

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.html

Department of Chemistry, University of Missouri–Columbia, 601 S. College Ave., Columbia, MO 65211 (USA) http://www.chem.missouri.edu/Harmata/synthesis.htmlSearch for more papers by this author
First published: 22 June 2012

Graphical Abstract

A Hydride Transfer that occurs by a 6-endo-trig process initiates an intramolecular redox reaction. In their Communication on page 7016 ff., M. Harmata et al. demonstrate that heating of N-alkyl-, N-allyl-, and N-benzyl-substituted S-alkenyl sulfoximines results in the formation of NH-S-alkyl sulfoximines under appropriate conditions. The intermediates in the reaction can also give access to four- and six-membered heterocyclic rings and a new class of chiral dienes.

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