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- W2045237449 abstract "Abstract The cycloaddition of ( Z )-1-methoxybut-1-en-3-yne ( 2 ) with 5,6-disubstituted 3-acylamino-2 H -pyran-2-ones 1 under microwave-irradiation conditions, with classical heating or at high-pressures (13–15 kbar) affords the benzene derivatives 3 with a strategically positioned 2-methoxyethenyl moiety. In some cases, at high-pressures after long reaction times, 2,2-dimethoxyethyl products 4 were obtained. Adducts 3 and 4 can be cyclized under mild conditions into 1,5,6-trisubstituted indole derivatives 5 ." @default.
- W2045237449 created "2016-06-24" @default.
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- W2045237449 date "2008-04-22" @default.
- W2045237449 modified "2023-10-07" @default.
- W2045237449 title "ChemInform Abstract: An Expedient Route to Indoles via a Cycloaddition/Cyclization Sequence from (Z)-1-Methoxybut-1-en-3-yne and 2H-Pyran-2-ones." @default.
- W2045237449 cites W2951702099 @default.
- W2045237449 doi "https://doi.org/10.1002/chin.200817119" @default.
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