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American Chemical Society, Journal of the American Chemical Society, 41(130), p. 13542-13543, 2008

DOI: 10.1021/ja806259z

Wiley-VCH Verlag, ChemInform, 7(40), 2009

DOI: 10.1002/chin.200907120

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Intramolecular Anodic Olefin Coupling Reactions: The Use of a Nitrogen Trapping Group

Journal article published in 2008 by Hai-Chao Xu ORCID, Kevin D. Moeller
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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Abstract

Anodic olefin coupling reactions using a tosylamine trapping group have been studied. The cyclizations are favored by the use of a less-polar radical cation and more basic reaction conditions. The most significant factor for obtaining good yields of cyclic product is the use of the more basic reaction conditions. The cyclizations allow for the rapid synthesis of substituted proline derivatives.