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 journalArticle

43 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 languageEnglish
Pages (from-to)3887-3893
Number of pages7
JournalTetrahedron Asymmetry
Volume8
Issue number23
DOIs
Publication statusPublished - Dec 11 1997
Externally publishedYes

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Alkaloids
glutamic acid
alkaloids
piperidine
Aldehydes
aldehydes
Glutamic Acid
Acids
synthesis

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Organic Chemistry
  • Materials Chemistry
  • Drug Discovery

Cite this

Asymmetric total syntheses of hydroxylated piperidine alkaloids via the intramolecular reaction of γ-aminoallylstannane with aldehyde. / Kadota, Isao; Kawada, Miho; Muramatsu, Yoko; Yamamoto, Yoshinori.

In: Tetrahedron Asymmetry, Vol. 8, No. 23, 11.12.1997, p. 3887-3893.

Research output: Contribution to journalArticle

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