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

Seetharamaiyer Padmanabhan; Kaustubh V. Gavaskar; David J. Triggle

doi:10.1080/00397919608004616

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

Seetharamaiyer Padmanabhan
, Kaustubh V. Gavaskar
, David J. Triggle

School of Pharmacy and Pharmaceutical Sciences

SUNY Buffalo
Bldg. #700

Research output: Contribution to journal › Article › peer-review

10 Scopus citations

Abstract

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.

Original language	English
Pages (from-to)	3109-3113
Number of pages	5
Journal	Synthetic Communications
Volume	26
Issue number	16
DOIs	https://doi.org/10.1080/00397919608004616
State	Published - 1996

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10.1080/00397919608004616

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title = "Reaction of iodoarenes and diethyl 2-pentenedicarboxylate under the heck reaction conditions. formation of 3-aryl-2-pentenedicarboxylates",

abstract = "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.",

author = "Seetharamaiyer Padmanabhan and Gavaskar, \{Kaustubh V.\} and Triggle, \{David J.\}",

year = "1996",

doi = "10.1080/00397919608004616",

language = "English",

volume = "26",

pages = "3109--3113",

journal = "Synthetic Communications",

issn = "0039-7911",

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T1 - Reaction of iodoarenes and diethyl 2-pentenedicarboxylate under the heck reaction conditions. formation of 3-aryl-2-pentenedicarboxylates

AU - Padmanabhan, Seetharamaiyer

AU - Gavaskar, Kaustubh V.

AU - Triggle, David J.

PY - 1996

Y1 - 1996

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/0029680669

U2 - 10.1080/00397919608004616

DO - 10.1080/00397919608004616

M3 - Article

AN - SCOPUS:0029680669

SN - 0039-7911

VL - 26

SP - 3109

EP - 3113

JO - Synthetic Communications

JF - Synthetic Communications

IS - 16

ER -

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

Abstract

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