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 language | English |
|---|---|
| Pages (from-to) | 1493-1506 |
| Number of pages | 14 |
| Journal | Heterocycles |
| Volume | 45 |
| Issue number | 8 |
| Publication status | Published - 1997 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
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 journal › Article
}
TY - JOUR
T1 - Synthesis of 5(10→9)abeo-ergolines
AU - Mantegani, Sergio
AU - Arlandini, Emanuele
AU - Borghi, Daniela
AU - Brambilla, Enzo
AU - Varasi, Mario
PY - 1997
Y1 - 1997
N2 - 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.
AB - 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.
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UR - http://www.scopus.com/inward/citedby.url?scp=0001509729&partnerID=8YFLogxK
M3 - Article
VL - 45
SP - 1493
EP - 1506
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 8
ER -