Mechanistic studies on Diels-Alder [4 + 2] cycloaddition reactions of α,β-substituted cyclobutenones: Role of substituents in regio- and stereoselectivity-Reference-Cited by-同舟云学术

Mechanistic studies on Diels-Alder [4 + 2] cycloaddition reactions of α,β-substituted cyclobutenones: Role of substituents in regio- and stereoselectivity

Published:2016-12 Issue:50 Volume:72 Page:8261-8273
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Fosu Evans,Tia Richard,Adei Evans

Funder

National Council for Tertiary Education

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

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2. Preparation and Diels−Alder Cycloaddition of 2-Acyloxyacroleins. Facile Synthesis of Functionalized Taxol A-Ring Synthons

3. Chiral auxiliary-mediated asymmetric induction in a thermal inverse electron demand hetero-Diels-Alder reaction. Enantioselective synthesis of the taxol A-ring side chain

4. Cyclobutenone as a Highly Reactive Dienophile: Expanding Upon Diels−Alder Paradigms

5. Synthesis of Highly Substituted Cyclohexenes via Mixed Lewis Acid-Catalyzed Diels−Alder Reactions of Highly Substituted Dienes and Dienophiles

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