Carbon-carbon bond formation using aromatics from biomass
Review article, 2024

The transition to a circular economy requires that we adapt currently used chemical processes to the structurally diverse and often highly oxygenated precursors that are accessible from biomass. In this review, we highlight different examples of carbon-carbon bond formation using aromatics derived from bio-based sources, reported during 2015-2024. Examples of sustainable biomass building blocks include heterocycles such as furfural and hydroxymethylfurfural, obtained from carbohydrates, as well as lignin-based aromatics such as vanillin and eugenol. These have subsequently been applied in a variety of different types of carbon-carbon bond formation, including more classical methods such as aldol condensation and Morita-Baylis-Hillman reactions, but also employing transition metal catalysis, electrochemistry or photochemistry to create new C-C bonds.

Author

Petter Dunås

Chalmers, Chemistry and Chemical Engineering, Chemistry and Biochemistry

Andrew Paterson

Chalmers, Chemistry and Chemical Engineering, Chemistry and Biochemistry

Simon E. Lewis

University of Bath

Nina Kann

Chalmers, Chemistry and Chemical Engineering, Chemistry and Biochemistry

Chemical Communications

1359-7345 (ISSN) 1364-548X (eISSN)

Vol. 60 100 14885-14895

Dearomatization and domino reactions as tools for the synthesis of functionalized polycyclic molecules

Swedish Research Council (VR) (2023-04342), 2024-01-01 -- 2027-12-31.

Subject Categories (SSIF 2011)

Organic Chemistry

DOI

10.1039/d4cc05664g

PubMed

39611735

More information

Latest update

1/9/2025 9