The simultaneous double Diels-Alder addition of 1,1-bis(3,5-dimethylfur-2-yl)ethane; toward a new, asymmetric synthesis of long-chain polypropionate fragments and analogues-Reference-Cited by-同舟云学术

The simultaneous double Diels-Alder addition of 1,1-bis(3,5-dimethylfur-2-yl)ethane; toward a new, asymmetric synthesis of long-chain polypropionate fragments and analogues

Published:1996-06 Issue:24 Volume:37 Page:4149-4152
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Marchionni Chiara,Vogel Pierre,Roversi Pietro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Total Synthesis of Bioactive Marine Macrolides

2. Synthesis of Polypropionate Fragments Containing Tertiary-Alcohol Moieties. Cross-aldolisations with lithium enolates of 7-oxabicyclo[2.2.1]heptan-2-one derivatives

3. See ref. 3–15, 17–22 in ref. [2]

4. A New Stereoselective and Convergent Approach to the Synthesis of Long-Chain Polypropionate Fragments

5. Diastereoselective aldol reactions of chiral aldehydes and chiral methyl ketones: Dependence of stereoselectivity on the metal enolate, the aldehyde 2,3-stereochemistry, and the aldehyde β-alkoxy protecting group

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1. Development and Applications of Double Diels‐Alder Reaction in Organic Synthesis;Asian Journal of Organic Chemistry;2021-10-05

2. Application of the Intramolecular Diels–Alder Vinylarenе (IMDAV) Approach for the Synthesis of Thieno[2,3-f]isoindoles;Synthesis;2020-03-12

3. Crystal structure and Hirshfeld surface analysis of dimethyl (1R*,3aS*,3a1 R*,6aS*,9R*,9aS*)-3a1,5,6,9a-tetrahydro-1H,4H,9H-1,3a:6a,9-diepoxyphenalene-2,3-dicarboxylate;Acta Crystallographica Section E Crystallographic Communications;2019-03-20

4. High Pressure, Temperature, and Solvent Effects on the Rate of the Diels-Alder Reaction of Furan with N-Phenylmaleimide;Russian Journal of Organic Chemistry;2019-01

5. Classical Example of Total Kinetic and Thermodynamic Control: The Diels–Alder Reaction between DMAD and Bis-furyl Dienes;The Journal of Organic Chemistry;2018-04-04