Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dennis Molendijk"'
Publikováno v:
Green Chemistry Letters and Reviews, Vol 13, Iss 4, Pp 349-364 (2020)
The formation of carbon–carbon bonds is a quest that has required a lot of research throughout the last 125 years of history of chemistry. The creation of these bonds is key to producing a wide variety of advanced products with great societal impor
Externí odkaz:
https://doaj.org/article/88bf83fbe6754a2aa0c523bf1bc60c8b
Autor:
Jack van Schijndel, Dennis Molendijk, Harmen Spakman, Edward Knaven, Luiz Alberto Canalle, Jan Meuldijk
Publikováno v:
Green Chemistry Letters and Reviews, Vol 12, Iss 3, Pp 323-331 (2019)
In the green Knoevenagel reaction of benzaldehyde and malonic acid, the carbon–carbon formation reaction is catalyzed by a double Schiff base formed by benzaldehyde and ammonia. A mechanism for this green Knoevenagel has been proposed. A closed cat
Externí odkaz:
https://doaj.org/article/470eb4c4f5494b43af2c94c83c9fd964
Publikováno v:
Green Chemistry Letters and Reviews, Vol 10, Iss 4, Pp 404-411 (2017)
This paper presents a novel, green Knoevenagel procedure for the chemical transformation of benzaldehydes into their corresponding α,β-unsaturated acids. The essential part of this procedure is a solvent-free condensation which uses environmentally
Externí odkaz:
https://doaj.org/article/97c84ffa6fbe4bb58d76176256034147
Publikováno v:
Green Chemistry Letters and Reviews, Vol 13, Iss 4, Pp 349-364 (2020)
The formation of carbon–carbon bonds is a quest that has required a lot of research throughout the last 125 years of history of chemistry. The creation of these bonds is key to producing a wide variety of advanced products with great societal impor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b545d0bf0683646f15746023e599d99
https://doi.org/10.1080/17518253.2020.1851398
https://doi.org/10.1080/17518253.2020.1851398
Publikováno v:
Journal of visualized experiments : JoVE. (165)
The development of chemically recyclable biopolymers offers opportunities within the pursuit of a circular economy. Chemically recyclable biopolymers make a positive effort to solve the issue of polymer materials in the disposal phase after the use p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0451511639504974c42f15867558b0f6
https://pubmed.ncbi.nlm.nih.gov/33311433
https://pubmed.ncbi.nlm.nih.gov/33311433
Autor:
Luiz Alberto Canalle, Koen van Beurden, J Jan Meuldijk, Dennis Molendijk, Jack van Schijndel, Timothy Noël
Publikováno v:
European Polymer Journal, 125:109534. Elsevier
Three different bio-based styrene monomer alternatives, i.e., 4-vinylphenol derivatives, were synthesized starting from lignin building blocks. The synthetic route encompassed a green Knoevenagel condensation followed by two decarboxylation steps and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d408d8af6531062481fc1e43d2085bd2
https://research.tue.nl/en/publications/d92728c2-98b4-4449-b7a6-ca4ed46d122b
https://research.tue.nl/en/publications/d92728c2-98b4-4449-b7a6-ca4ed46d122b
Publikováno v:
Synlett, 29(15):st-2018-b0227-l, 1983-1988. Georg Thieme Verlag KG
This paper presents mechanistic considerations on an efficient, green, and solvent-free Knoevenagel procedure for the chemical transformation of furanic aldehydes into their corresponding α,β-unsaturated compounds. In the proposed mechanism furanic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52cc915bf995ca6e5b2ab264b6015dcc
https://research.tue.nl/nl/publications/41edc18e-8242-491c-9424-6e960d122c44
https://research.tue.nl/nl/publications/41edc18e-8242-491c-9424-6e960d122c44
