2006
DOI: 10.1039/b517631j
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The photomediated reaction of alkynes with cycloalkanes

Abstract: In the presence of a photomediator such as benzophenone, alkynes with electron-withdrawing groups react with cycloalkanes to give vinyl cycloalkanes. The reaction involves the regiospecific addition of a photochemically generated cycloalkyl radical to the beta-carbon of the alkyne. The stereochemical outcome of the reaction depends on the nature of the photomediator and alkyne used.

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Cited by 27 publications
(18 citation statements)
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“…Methyl cyclobutenecarboxylates 4–6 a and related norbornene‐derived compounds 7–9 a were prepared following the reported procedure . 2‐Methoxyethyl propiolate 2 was prepared via Mitsunobu esterification of propiolic acid with 2‐methoxyethanol. Preparation of 3‐γ‐butyrolactonyl propiolate 3 was reported in our previous publication …”
Section: Methodsmentioning
confidence: 99%
“…Methyl cyclobutenecarboxylates 4–6 a and related norbornene‐derived compounds 7–9 a were prepared following the reported procedure . 2‐Methoxyethyl propiolate 2 was prepared via Mitsunobu esterification of propiolic acid with 2‐methoxyethanol. Preparation of 3‐γ‐butyrolactonyl propiolate 3 was reported in our previous publication …”
Section: Methodsmentioning
confidence: 99%
“…70:30 from the corresponding aldehydes 12a-e by Horner-Wadsworth-Emmons olefination employing ethyl (di-o-tolylphosphono)acetate (Scheme 3). Subsequent reduction to the respective allyl alcohol with DIBAL in THF at -78°C, followed by oxidation with MnO 2 in hexane at room temperature gave the target (2Z)-alkenals (Z)-10a, [28] (Z)-10b, [29] and (Z)-10c-e.…”
Section: Synthesis Of (Z)-αβ-unsaturated Aldehydes (Z)-10a-ementioning
confidence: 99%
“…The reaction involves the regiospecific addition of a photochemically generated cycloalkyl radical to the β ‐carbon of the alkyne. [ 80 ]…”
Section: Synthetic Strategies Of Acrylonitrilesmentioning
confidence: 99%