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Optimized syntheses of the furan fatty acids F5 and F6 featuring convertion of a β-iodofuran into a β-methylfuran in a single operation

Knight, David William and Smith, Andrew William T. 2012. Optimized syntheses of the furan fatty acids F5 and F6 featuring convertion of a β-iodofuran into a β-methylfuran in a single operation. Heterocycles 84 (1) , pp. 361-369. 10.3987/COM-11-S(P)63

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Abstract

Optimized syntheses of the furan fatty acids F5 1a and F6 1b are described, which give >60% overall yields over 7 or 8 steps respectively starting from 10-undecenal 6. The F6 approach also features a conversion of a β-iodofuran into the corresponding β-methyl derivative in a single operation.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Cardiff Catalysis Institute (CCI)
Subjects: Q Science > QD Chemistry
Uncontrolled Keywords: Furan; Fatty Acid; Synthesis; endo-Dig; Iodine-Methyl Exchange
Publisher: Sendai Institute of Heterocyclic Chemistry
ISSN: 0385-5414
Last Modified: 04 Jun 2017 03:46
URI: http://orca.cf.ac.uk/id/eprint/26349

Cited 2 times in Web of Science. View in Web of Science.

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