Overman rearrangement of γ-aryl crotyl alcohols: Effects of aryl substituents

Article abstract of DOI:10.1080/00397910008087201

Various α,α'-methyl aryl allylic amines were synthesized from γ-aryl crotyl alcohols via thermal Overman rearrangement. Noteworthy is that the presence of the electron withdrawing groups at aryl group causes substantial increases in the reaction rates and

Full text of DOI:10.1080/00397910008087201

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Overman Rearrangement of γ-
Aryl Crotyl Alcohols: Effects of
Aryl Substituents
Cheon-Gyu Cho a , Yeong-Kwan Lira a , Kang-Sang
Lee a , In-Hak Jung a & Moon-Yeong Yoon a
a Department of Chemistry , Hanyang University ,
Seoul, 131-791, Korea
Published online: 04 Dec 2007.
To cite this article: Cheon-Gyu Cho , Yeong-Kwan Lira , Kang-Sang Lee , In-Hak
Jung & Moon-Yeong Yoon (2000) Overman Rearrangement of γ- Aryl Crotyl Alcohols:
Effects of Aryl Substituents, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 30:9, 1643-1650, DOI:
10.1080/00397910008087201
To link to this article: http://dx.doi.org/10.1080/00397910008087201
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