Synthesis of 5(10→9)abeo-ergolines

Sergio Mantegani, Emanuele Arlandini, Daniela Borghi, Enzo Brambilla, Mario Varasi

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Reaction of the (5 R, 8 R)-ergoline derivative (6) with the couple CCl4/(Ph)3P unexpectedly resulted in the formation of the novel (5 S, 8 R)-5 (10→9)abeo-ergoline derivative. A mechanism of this transposition process is proposed.

Original languageEnglish
Pages (from-to)1493-1506
Number of pages14
JournalHeterocycles
Volume45
Issue number8
Publication statusPublished - 1997

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Ergolines
Derivatives

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Mantegani, S., Arlandini, E., Borghi, D., Brambilla, E., & Varasi, M. (1997). Synthesis of 5(10→9)abeo-ergolines. Heterocycles, 45(8), 1493-1506.

Synthesis of 5(10→9)abeo-ergolines. / Mantegani, Sergio; Arlandini, Emanuele; Borghi, Daniela; Brambilla, Enzo; Varasi, Mario.

In: Heterocycles, Vol. 45, No. 8, 1997, p. 1493-1506.

Research output: Contribution to journalArticle

Mantegani, S, Arlandini, E, Borghi, D, Brambilla, E & Varasi, M 1997, 'Synthesis of 5(10→9)abeo-ergolines', Heterocycles, vol. 45, no. 8, pp. 1493-1506.
Mantegani S, Arlandini E, Borghi D, Brambilla E, Varasi M. Synthesis of 5(10→9)abeo-ergolines. Heterocycles. 1997;45(8):1493-1506.
Mantegani, Sergio ; Arlandini, Emanuele ; Borghi, Daniela ; Brambilla, Enzo ; Varasi, Mario. / Synthesis of 5(10→9)abeo-ergolines. In: Heterocycles. 1997 ; Vol. 45, No. 8. pp. 1493-1506.
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