Novel Synthetic Approach Toward (±)-β-Cuparenone via Palladium-Catalyzed Tandem Heck Cyclization of 1-Bromo-5-methyl-1-aryl-hexa-1,5-dien-3-ol Derivatives
Author:
Affiliation:
1. Department of Chemistry, Indian Institute of Technology, Kharagpur 721302, India
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol062418t
Reference15 articles.
1. Palladium-catalyzed tandem oxidative cyclization of 1-bromohexa-1,5-dien-3-ols: easy access to cyclopentenones
2. Palladium-Catalyzed Novel Cycloisomerization: An Unprecedented Domino Oxidative Cyclization towards Substituted Carbocycles
3. Asymmetric Approach to (+)-β-Cuparenone by Intramolecular Pauson−Khand Reaction
4. Radical cyclization strategies to terpenoids; syntheses of (±)-β-cuparenone, (±)-laurene and epilaurenes
5. Total synthesis of the sesquiterpene (±)β-cuparenone: use of three-carbon annulation in synthesis
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