期刊
GREEN CHEMISTRY
卷 15, 期 6, 页码 1514-1519出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3gc40358k
关键词
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资金
- FAPESP [2012/00124-9]
- CAPES [707/2012]
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [12/00124-9] Funding Source: FAPESP
The bulk reaction of 2-furfuryl amine with epoxidized linseed oil took place at both its ester moieties (aminolysis) and oxirane groups (ring opening) producing three fatty acid furan amides incorporating further furan heterocycles along their chains. These reactions were followed spectroscopically and the ensuing monomers used in Diels-Alder reversible polycondensations.
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