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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A straightforward double coupling of furan moieties onto epoxidized triglycerides: synthesis of monomers based on two renewable resources

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Author(s):
Gandini, Alessandro [1, 2] ; Lacerda, Talita M. [1, 2] ; Carvalho, Antonio J. F. [2]
Total Authors: 3
Affiliation:
[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13566590 Sao Carlos, SP - Brazil
[2] Univ Sao Paulo, Escola Engn, BR-13566590 Sao Carlos, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: GREEN CHEMISTRY; v. 15, n. 6, p. 1514-1519, 2013.
Web of Science Citations: 18
Abstract

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. (AU)

FAPESP's process: 12/00124-9 - Synthesis and thermal-reversible polymerization of macromonomers derived from vegetal oil and furan.
Grantee:Talita Martins Lacerda
Support Opportunities: Scholarships in Brazil - Post-Doctoral