Diels–Alder reaction of vinylene carbonate and 2,5-dimethylfuran: kinetic vs. thermodynamic control-Reference-Cited by-同舟云学术

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Diels–Alder reaction of vinylene carbonate and 2,5-dimethylfuran: kinetic vs. thermodynamic control

Published:2010 Issue:3 Volume:34 Page:517
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Taffin Céline,Kreutler Glenda,Bourgeois Damien,Clot Eric,Périgaud Christian

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2010/NJ/B9NJ00536F

Reference38 articles.

1. Synthetic applications of furan Diels-Alder chemistry

2. Five-membered heteroaromatic rings as intermediates in organic synthesis

3. Thermal and catalytic intramolecular [4+2]-cycloaddition in 2-alkenylfurans

4. Derivatives of 7-oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediates

5. Synthesen in der hydro‐aromatischen Reihe, II. Mitteilung: Über Cantharidin

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2. Chemical upcycling of poly(bisphenol A carbonate) to vinylene carbonates through organocatalysis;Green Chemistry;2023

3. Recent Progress in C—H Bond Activation Reaction with Vinylene Carbonate;Chinese Journal of Organic Chemistry;2023

4. Theoretical survey of Diels-Alder between acrylic acid and isoprene catalyzed by the titanium tetrachloride and titanium tertafluoride;Journal of Molecular Structure;2022-12

5. Direct Synthesis of Vinylene Carbonates from Aromatic Aldehydes**;European Journal of Organic Chemistry;2022-03-24

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