Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/15490
Title: Novel synthesis of o-naphthothiophenequinone derivatives via regioselective Diels-Alder reaction
Authors: Shen, YD
Wu, HQ
Zhang, SL
Bu, XZ
An, LK
Huang, ZS
Liu, PQ
Gu, LQ
Li, YM
Chan, ASC
Keywords: Diels-Alder
IBX
o-Naphthothiophenequinone
Regioselectivity
Issue Date: 2005
Publisher: Pergamon Press
Source: Tetrahedron, 2005, v. 61, no. 38, p. 9097-9101 How to cite?
Journal: Tetrahedron 
Abstract: A novel procedure to construct o-naphthothiophenequinones has been achieved from readily available o-benzothiophenquinones and N-dienes via Diels-Alder reaction-aromatization sequence as key steps. The absolute regioselectivity was established via Diels-Alder reaction of o-benzothiophenquinones with rich electron N-dienes.
URI: http://hdl.handle.net/10397/15490
ISSN: 0040-4020
DOI: 10.1016/j.tet.2005.07.036
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