Novel method for the synthesis of α- and β-halogenonaphthalenes by regioselective benzannulation of aryl(gem-dihalogenocyclopropyl)methanols: application to the total synthesis of the lignan lactones, justicidin E and taiwanin C1-Reference-Cited by-同舟云学术

Novel method for the synthesis of α- and β-halogenonaphthalenes by regioselective benzannulation of aryl(gem-dihalogenocyclopropyl)methanols: application to the total synthesis of the lignan lactones, justicidin E and taiwanin C1

Published:1996 Issue:17 Volume: Page:2157-2165
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Tanabe Yoo,Seko Shinzo,Nishii Yoshinori,Yoshida Taichi,Utsumi Naoka,Suzukamo Gohfu

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1996/P1/P19960002157

Reference66 articles.

1. A novel synthesis of α- and β-halonaphthalenes via regioselective ring cleavage of aryl(gem-dihalocyclopropyl)methanols and its application to total synthesis of lignan lactones, justicidin e and taiwanin c

2. Use of cyclopropanes and their derivatives in organic synthesis

3. Donor-acceptor-substituted cyclopropanes: Versatile building blocks in organic synthesis

4. Chemical activation of host defence mechanisms as a basis for crop protection

5. Structural and biological link between pyrethroids and DDT in new insecticides

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