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• W2314469191 abstract "Abstract magnified image N ‐ p ‐Toluenesulfonyl‐3‐vinylpyrrole underwent endo ‐addition [4 + 2] cycloaddition reactions with maleimides and benzoquinones, followed by isomerization to give tetrahydroindoles in good yields. Dehydrogenation with activated MnO 2 in refluxing toluene gave the corresponding indoles in fair to good yields. Detosylation via saponification or with magnesium in refluxing methanol gave the N ‐H indoles in moderate to good yields. This method for formation of indoles is both convergent and versatile and uses starting materials that are conveniently prepared. J. Heterocyclic Chem., (2009)." @default.
• W2314469191 created "2016-06-24" @default.
• W2314469191 creator A5032859403 @default.
• W2314469191 creator A5049552223 @default.
• W2314469191 date "2009-11-01" @default.
• W2314469191 modified "2023-10-18" @default.
• W2314469191 title "Access to indoles<i>via</i>Diels-Alder reactions of 3-vinylpyrroles" @default.
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• W2314469191 doi "https://doi.org/10.1002/jhet.228" @default.
• W2314469191 hasPublicationYear "2009" @default.
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