Synthesis of 2-Acetyl-5,8-dihydro-1,4-dihydroxy-3-methyl Naphthalene: A Product from the Isomerisation of Diels-Alder Adducts of Both 5-Methyl- and 6-Methyl-2-acetyl-1,4-benzoquinone with 1,3-Butadiene-Reference-Cited by-同舟云学术

Synthesis of 2-Acetyl-5,8-dihydro-1,4-dihydroxy-3-methyl Naphthalene: A Product from the Isomerisation of Diels-Alder Adducts of Both 5-Methyl- and 6-Methyl-2-acetyl-1,4-benzoquinone with 1,3-Butadiene

Published:1996-04 Issue:7 Volume:26 Page:1263-1271
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Ahmad Faujan B. H.,Bruce J. Malcolm

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397919608003486

Reference5 articles.

1. [1,5] and [1,2] Acetyl shifts in Diels–Alder adducts of 2-acetyl-6-methyl-1,4-benzoquinone

2. Isomerization of Diels-Alder Adducts of Benzoyl-1,4-benzoquinones: A Route to the Anthracyclinone Ring system

3. 194. A synthesis of vitamin a from cyclohexanone

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4. ChemInform Abstract: Synthesis of 2-Acetyl-5,8-dihydro-1,4-dihydroxy-3-methyl Naphthalene: A Product from the Isomerization of Diels-Alder Adducts of Both 5- Methyl- and 6-Methyl-2-acetyl-1,4-benzoquinone with 1,3-Butadiene.;ChemInform;2010-08-05

5. Compounds derived from acetic acid;Handbook of Hydroxyacetophenones: Preparation and Physical Properties;2005