Redox-photosensitised reactions. Part 6. Stereospecific ring cleavage of 1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobuta[a]naphthalene-8b-carbonitrile and its 2-methyl derivatives by redox-photosensitisation-Reference-Cited by-同舟云学术

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Redox-photosensitised reactions. Part 6. Stereospecific ring cleavage of 1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobuta[a]naphthalene-8b-carbonitrile and its 2-methyl derivatives by redox-photosensitisation

Published:1980 Issue: Volume: Page:2705
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Majima Tetsuro,Pac Chyongjin,Sakurai Hiroshi

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1980/P1/P19800002705

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2. Easy access to enamides: a mild nickel-catalysed alkene isomerization of allylamides;Chemical Communications;2013

3. Photoreactions of 1,2,4,5-benzenetetracarbonitrile with arylethenes—photo- olefin dimerization–aromatic substitution reactions;Tetrahedron;2006-06

4. Highly selective isomerization of N-allylamides catalyzed by ruthenium and rhodium complexes;Journal of Molecular Catalysis A: Chemical;2005-01

5. Highly selective isomerization of N-allylamides and N-allylamines;Tetrahedron Letters;2004-06

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