Autocatalytic Domino Michael Reaction Leading to Bicyclo[2.2.2]octane-2,5-dione Derivatives-Reference-Cited by-同舟云学术

Autocatalytic Domino Michael Reaction Leading to Bicyclo[2.2.2]octane-2,5-dione Derivatives

Published:2004-03-06 Issue:7 Volume:6 Page:1115-1118
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hagiwara Hisahiro¹,Endou Satoru¹,Fukushima Masakazu¹,Hoshi Takashi¹,Suzuki Toshio¹

Affiliation:

1. Graduate School of Science and Technology, Niigata University, 8050, 2-Nocho, Ikarashi, Niigata 950-2181, Japan, and Faculty of Engineering, Niigata University, 8050, 2-Nocho, Ikarashi, Niigata 950-2181, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol049948e

Reference11 articles.

1. Sequential Transformations in Organic Chemistry: A Synthetic Strategy with a Future

2. Reactions of α′ dienolates with michael acceptors: a synthesis of bicyclo [2,2,2] octan-2-ones.

3. Convergent Enantioselective Synthesis of Vinigrol, an Architecturally Novel Diterpenoid with Potent Platelet Aggregation Inhibitory and Antihypertensive Properties. 1. Application of Anionic Sigmatropy to Construction of the Octalin Substructure

4. Lewis acid catalyzed Diels-Alder reactions of 3-methyl-1-(triisopropylsiloxy)-1,3-cyclohexadiene: factors influencing the stereoselectivity

5. First Total Syntheses of the Phytotoxins Solanapyrones D and E via the Domino Michael Protocol

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