Total synthesis of (+)-desoxoprosopinine via the intramolecular reaction of γ-aminoallylstannane

Isao Kadota, Miho Kawada, Yoko Muramatsu, Yoshinori Yamamoto

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

A stereoselective total synthesis of (+)-desoxoprosopinine starting from L-glutamic acid as a chiral source was accomplished in which the intramolecular reaction of γ-aminoallylstannane with aldehyde was used as a key step.

Original languageEnglish
Pages (from-to)7469-7470
Number of pages2
JournalTetrahedron Letters
Volume38
Issue number42
DOIs
Publication statusPublished - Oct 20 1997
Externally publishedYes

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Aldehydes
Glutamic Acid

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Total synthesis of (+)-desoxoprosopinine via the intramolecular reaction of γ-aminoallylstannane. / Kadota, Isao; Kawada, Miho; Muramatsu, Yoko; Yamamoto, Yoshinori.

In: Tetrahedron Letters, Vol. 38, No. 42, 20.10.1997, p. 7469-7470.

Research output: Contribution to journalArticle

Kadota, Isao ; Kawada, Miho ; Muramatsu, Yoko ; Yamamoto, Yoshinori. / Total synthesis of (+)-desoxoprosopinine via the intramolecular reaction of γ-aminoallylstannane. In: Tetrahedron Letters. 1997 ; Vol. 38, No. 42. pp. 7469-7470.
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