Asymmetric total syntheses of hydroxylated piperidine alkaloids via the intramolecular reaction of γ-aminoallylstannane with aldehyde

Isao Kadota; Miho Kawada; Yoko Muramatsu; Yoshinori Yamamoto

doi:10.1016/S0957-4166(97)00563-6

Asymmetric total syntheses of hydroxylated piperidine alkaloids via the intramolecular reaction of γ-aminoallylstannane with aldehyde

Isao Kadota, Miho Kawada, Yoko Muramatsu, Yoshinori Yamamoto

Research output: Contribution to journal › Article › peer-review

45 Citations (Scopus)

Abstract

Asymmetric total syntheses of (+)-desoxoprosopinine and (-)- desoxoprosophylline were accomplished, using L-glutamic acid as the chiral source, in which the intramolecular reaction of a γ-aminoallylstannane with an aldehyde was used as a key step.

Original language	English
Pages (from-to)	3887-3893
Number of pages	7
Journal	Tetrahedron Asymmetry
Volume	8
Issue number	23
DOIs	https://doi.org/10.1016/S0957-4166(97)00563-6
Publication status	Published - Dec 11 1997
Externally published	Yes

ASJC Scopus subject areas

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1016/S0957-4166(97)00563-6

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title = "Asymmetric total syntheses of hydroxylated piperidine alkaloids via the intramolecular reaction of γ-aminoallylstannane with aldehyde",

abstract = "Asymmetric total syntheses of (+)-desoxoprosopinine and (-)- desoxoprosophylline were accomplished, using L-glutamic acid as the chiral source, in which the intramolecular reaction of a γ-aminoallylstannane with an aldehyde was used as a key step.",

author = "Isao Kadota and Miho Kawada and Yoko Muramatsu and Yoshinori Yamamoto",

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AU - Kadota, Isao

AU - Kawada, Miho

AU - Muramatsu, Yoko

AU - Yamamoto, Yoshinori

PY - 1997/12/11

Y1 - 1997/12/11

N2 - Asymmetric total syntheses of (+)-desoxoprosopinine and (-)- desoxoprosophylline were accomplished, using L-glutamic acid as the chiral source, in which the intramolecular reaction of a γ-aminoallylstannane with an aldehyde was used as a key step.

AB - Asymmetric total syntheses of (+)-desoxoprosopinine and (-)- desoxoprosophylline were accomplished, using L-glutamic acid as the chiral source, in which the intramolecular reaction of a γ-aminoallylstannane with an aldehyde was used as a key step.

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U2 - 10.1016/S0957-4166(97)00563-6

DO - 10.1016/S0957-4166(97)00563-6

M3 - Article

AN - SCOPUS:0031466885

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JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

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ER -

Asymmetric total syntheses of hydroxylated piperidine alkaloids via the intramolecular reaction of γ-aminoallylstannane with aldehyde

Abstract

ASJC Scopus subject areas

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