(Q104973540)

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A new enantioselective route to the Sceletium alkaloids via a cyclopentanone–cyclohexenone transformation

scientific article published on 26 March 2003

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A new enantioselective route to the Sceletium alkaloids via a cyclopentanone–cyclohexenone transformation (English)

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main subject

Mesembryanthemum ladismithiense

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Mesembryanthemum tortuosum

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3a-(3,4-Dimethoxyphenyl)-1-methyl-2,3,4,5,7,7a-hexahydroindol-6-one

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Mesembryanthemum expansum

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Mesembryanthemum emarcidum

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Masato Hayashi

1

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Tomohiro Unno

series ordinal

2

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Michiyasu Takahashi

series ordinal

3

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Kunio Ogasawara

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4

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publication date

February 2002

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16 September 2022

16 September 2022

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volume

43

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issue

8

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page(s)

1461-1464

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cites work

Lanthanoids in organic synthesis. 6. Reduction of .alpha.-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspects

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7 January 2021

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CLAISEN'sche Umlagerungen bei Allyl- und Benzylalkoholen mit Hilfe von Acetalen des N, N-Dimethylacetamids. Vorläufige Mitteilung

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7 January 2021

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A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species

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https://api.crossref.org/works/10.1016%2FS0040-4039%2802%2900033-3

retrieved

7 January 2021

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Diastereoselective synthesis of 3,4-dimethoxy-7-morphinanone: a potential route to morphine

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https://api.crossref.org/works/10.1016%2FS0040-4039%2802%2900033-3

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7 January 2021

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Identifiers

DOI

10.1016/S0040-4039(02)00033-3

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(Q104973540)

A new enantioselective route to the Sceletium alkaloids via a cyclopentanone–cyclohexenone transformation

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