1995
DOI: 10.1055/s-1995-4996
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Palladium-catalyzed Annulation of Oxygen-Substituted 1,3-Dienes

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Cited by 51 publications
(18 citation statements)
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“…2-Aminophenylpalladium complexes appear to be intermediates in the palladium-catalysed formation of nitrogencontaining heterocycles from o-iodo-or o-bromoanilines and, for example, alkynes, [14±17] dienes, [18] or vinyl cyclopropanes and cyclobutanes, [19] as well as in intramolecular cascade cyclizations.…”
Section: Introductionmentioning
confidence: 99%
“…2-Aminophenylpalladium complexes appear to be intermediates in the palladium-catalysed formation of nitrogencontaining heterocycles from o-iodo-or o-bromoanilines and, for example, alkynes, [14±17] dienes, [18] or vinyl cyclopropanes and cyclobutanes, [19] as well as in intramolecular cascade cyclizations.…”
Section: Introductionmentioning
confidence: 99%
“…Itahara and others [79][80][81][82][83][84][85][86] have reported the palladium-assisted synthesis of these indoles.The heteroannulation of N-tosyl-2-iodoaniline with a variety of oxygen substituted 1,3 dienes has been described by Larock and Guo [87].…”
Section: Synthesis Of Indolinesmentioning
confidence: 98%
“…[32] This system has also been formed as minor byproducts of radical homoallylation, [33] insertion of a triple bond into a C À H bond of an olefin in arene-chromium tricarbonyl complexes, [34] and Pd-catalyzed annulation of O-substituted 1,3-dienes. [35] Asymmetric synthesis of trans-pterocarpin: The last stage was to check the applicability of the method to the asymmetric total synthesis of natural pterocarpans. Here, we describe the enantioselective total synthesis of (À)-trans-pterocarpin and its isomerization into the natural (À)-cis-pterocarpin.…”
Section: Full Papermentioning
confidence: 99%