Diels-Alder reactions of 1,3-dienylboronates as a new route to functionalized carbocycles.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Allyl silanes in organic synthesis: some reactions of 3-trimethylsilylcyclohex-4-ene-1,2-dicarboxylic acid and its derivatives
2. Regioselectivity in the Diels–Alder reaction of 1-trimethylsilylbutadiene
3. Regiospecific cycloaddition reactions using functionalized isoprenylsilane and related compounds
4. A regioselective synthesis of 2-tributylstannyl-1,3-dienes
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1. Facile access to 1,3-bis(boryl) dienes to build molecular complexity through cycloadditions;Tetrahedron Letters;2023-03
2. Synthesis, Biosynthesis, and Biological Activity of Diels–Alder Adducts from Morus Genus: An Update;Molecules;2022-11-04
3. Preparation of Dienyl Boronates by Tandem Ene–Yne Metathesis/Dienyl Isomerization: Ready Access to Diene Building Blocks for the Synthesis of Polyenes;The Journal of Organic Chemistry;2022-10-12
4. Regioselectivity Switch Towards the Development of Innovative Diels‐Alder Cycloaddition and Productive Applications in Organic Synthesis;Asian Journal of Organic Chemistry;2022-03-04
5. Generating Skeletal Diversity and Complexity from Boron-Substituted 1,3-Dienes and Enophiles;European Journal of Organic Chemistry;2020-05-27
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