The first intramolecular Heck–Matsuda reaction and its application in the syntheses of benzofurans and indoles

Siqueira, Fernanda Amaral de; Taylor, Jason G.; Correia, Carlos Roque Duarte

doi:10.1016/j.tetlet.2010.02.011

Cited by 56 publications

(19 citation statements)

References 38 publications

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“…Correia et al recently reported the first example of a series of intramolecular Matsuda-Heck reactions [57]. With this report in mind, the Heck reaction was attempted on tetrafluoroborate 140.…”

mentioning

confidence: 89%

Selectivity in the Synthesis of Cyclic Sulfonamides

Geoghegan¹

2014

Springer Theses

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The series "Springer Theses" brings together a selection of the very best Ph.D. theses from around the world and across the physical sciences. Nominated and endorsed by two recognized specialists, each published volume has been selected for its scientific excellence and the high impact of its contents for the pertinent field of research. For greater accessibility to non-specialists, the published versions include an extended introduction, as well as a foreword by the student's supervisor explaining the special relevance of the work for the field. As a whole, the series will provide a valuable resource both for newcomers to the research fields described, and for other scientists seeking detailed background information on special questions. Finally, it provides an accredited documentation of the valuable contributions made by today's younger generation of scientists.Theses are accepted into the series by invited nomination only and must fulfill all of the following criteria • They must be written in good English.• The topic should fall within the confines of Chemistry, Physics, Earth Sciences, Engineering and related interdisciplinary fields such as Materials, Nanoscience, Chemical Engineering, Complex Systems and Biophysics.

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confidence: 89%

Selectivity in the Synthesis of Cyclic Sulfonamides

Geoghegan¹

2014

Springer Theses

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“…However, Barluenga and coworkers effected a novel one-pot indole synthesis from o-haloanilines and alkenyl halides (Scheme 3, equation 1) [37]. Correia and colleagues parlayed a Heck-Matsuda reaction to an indole synthesis (equation 3) [39]. Similarly, 2-substituted indoles were prepared employing 1-substituted alkenyl bromides.…”

Section: The Mori-ban Indole Synthesis Is a Pd-catalyzed Cyclization mentioning

confidence: 99%

Palladium‐Catalyzed Indole Ring Synthesis

Gribble

2016

Indole Ring Synthesis

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“…54 Carbonylative Heck cyclisation of aryldiazonium salts 58 onto pendant alkenes was shown to give DHBs 59 containing a carboxylic acid group on the C 3 side chain in moderate yield. 55 Using aryl bromide 60, a series of Pd-catalysed tandem cyclisation/coupling reactions were investigated. 56 For example, tandem cyclisation/Stille coupling yielded 3,3-disubstituted DHB 61 in good yield in the presence of 1,3-dimethyl-1,2-imidazolidinone (DMI).…”

Section: Formation Of the Aryl-c 3 Bondmentioning

confidence: 99%