Reaction of iodoarenes and diethyl 2-pentenedicarboxylate under the Heck reaction conditions. Formation of 3-aryl-2-pentenedicarboxylates

Article abstract of DOI:10.1080/00397919608004616

Various substituted iodoarenes underwent arylation with diethyl 2-pentenedicarboxylate under the Heck reaction conditions to give the expected diethyl 3-aryl-2-pentenedicarboxylates. Extension of this reaction to 2-iodoaniline gave the hitherto unreported ethyl quinolin-2-one-4-acetate.

Full text of DOI:10.1080/00397919608004616

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Reaction of Iodoarenes and
Diethyl 2-Pentenedicarboxylate
Under the Heck Reaction
Conditions. Formation of 3-
Aryl-2-pentenedicarboxylates
Seetharamaiyer Padmanabhan a , Kaustubh V.
Gavaskar a & David J. Triggle a
a Departments of Biochemical Pharmacology and
Medicinal Chemistry, School of Pharmacy, State
University of New York at Buffalo, Buffalo, NY,
14260, USA
Available online: 21 Aug 2006
To cite this article: Seetharamaiyer Padmanabhan, Kaustubh V. Gavaskar & David J.
Triggle (1996): Reaction of Iodoarenes and Diethyl 2-Pentenedicarboxylate Under the
Heck Reaction Conditions. Formation of 3-Aryl-2-pentenedicarboxylates, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:16, 3109-3113
To link to this article: http://dx.doi.org/10.1080/00397919608004616
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