Isomerization of 7-Oxabenzonorbornadienes into Naphthols Catalyzed by [RuCl2(CO)3]2-Reference-Cited by-同舟云学术

Isomerization of 7-Oxabenzonorbornadienes into Naphthols Catalyzed by [RuCl2(CO)3]2

Published:2009-09-02 Issue:19 Volume:74 Page:7570-7573
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ballantine Melissa¹,Menard Michelle L.¹,Tam William¹

Affiliation:

1. Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, Department of Chemistry, University of Guelph, Guelph, Ontario, Canada N1G 2W1

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo901504n

Reference34 articles.

1. New Catalytic Reactions of Oxa- and Azabicyclic Alkenes

2. Transition Metal-Catalyzed Enantioselective Ring-Opening Reactions of Oxabicyclic Alkenes

3. Synthesis of the Tetracyclic Framework of the Erythrina Alkaloids Using a [4 + 2]-Cycloaddition/Rh(I)-Catalyzed Cascade of 2-Imidofurans

4. Rhodium-Catalyzed Ring-Opening Reactions of N-Boc-Azabenzonorbornadienes with Amine Nucleophiles

5. Pd-Catalyzed Ring Opening of Oxa- and Azabicyclic Alkenes with Aryl and Vinyl Halides: Efficient Entry to 2-Substituted 1,2-Dihydro-1-naphthols and 2-Substituted 1-Naphthols

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