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Synthesis of bicyclo [2.2.2] octenols via ni (0) -catalyzed alkylative cyclization of multi-functional aldehydes
Joint Authors
al-Douhaibi, Ahmad Samih
Montgomeryb, John
Source
Issue
Vol. 6, Issue 2 (30 Jun. 2011), pp.123-138, 16 p.
Publisher
Yarmouk University Deanship of Research and Graduate Studies
Publication Date
2011-06-30
Country of Publication
Jordan
No. of Pages
16
Main Subjects
Topics
Abstract EN
Nickel-catalyzed three-component coupling reactions of α, β, γ, δ-unsaturated dienals, alkynes, and alkynyltin reagents to produce more functionalized aldehydes have been achieved.
The aldehydes produced were subjected to a Ni (0)-catalyzed alkylative cyclization reaction to provide direct access to highly functionalized bicyclo [2.2.2] octenols.
In addition to their existence as substructures of complex natural molecules, these compounds possess interesting stereo chemical properties, and can be interesting three-dimensional scaffolds for library design.
American Psychological Association (APA)
al-Douhaibi, Ahmad Samih& Montgomeryb, John. 2011. Synthesis of bicyclo [2.2.2] octenols via ni (0) -catalyzed alkylative cyclization of multi-functional aldehydes. Jordan Journal of Chemistry،Vol. 6, no. 2, pp.123-138.
https://search.emarefa.net/detail/BIM-264418
Modern Language Association (MLA)
al-Douhaibi, Ahmad Samih& Montgomeryb, John. Synthesis of bicyclo [2.2.2] octenols via ni (0) -catalyzed alkylative cyclization of multi-functional aldehydes. Jordan Journal of Chemistry Vol. 6, no. 2 (Jun. 2011), pp.123-138.
https://search.emarefa.net/detail/BIM-264418
American Medical Association (AMA)
al-Douhaibi, Ahmad Samih& Montgomeryb, John. Synthesis of bicyclo [2.2.2] octenols via ni (0) -catalyzed alkylative cyclization of multi-functional aldehydes. Jordan Journal of Chemistry. 2011. Vol. 6, no. 2, pp.123-138.
https://search.emarefa.net/detail/BIM-264418
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 138
Record ID
BIM-264418