SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE
1
a Lilly Research Laboratories Eli Lilly and Company , Indianapolis, IN, 46285
|
Publication type: Journal Article
Publication date: 1990-12-01
scimago Q3
wos Q3
SJR: 0.322
CiteScore: 4.3
Impact factor: 1.8
ISSN: 00397911, 15322432
Organic Chemistry
Abstract
Abstract A convenient synthesis and resolution of (-)-trans-4aR,8aR-1-propyl-6-oxo-decahydroquinoline (4) is described. This compound is then converted into the D-2 selective dopamine agonist, (-)-quinpirole hydrochloride (3).
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20
Total citations:
20
Citations from 2024:
2
(10%)
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MLA
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GOST
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Schaus J. M., Huser D. L., Titus R. D. SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE // Synthetic Communications. 1990. Vol. 20. No. 22. pp. 3553-3562.
GOST all authors (up to 50)
Copy
Schaus J. M., Huser D. L., Titus R. D. SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE // Synthetic Communications. 1990. Vol. 20. No. 22. pp. 3553-3562.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1080/00397919008051599
UR - https://doi.org/10.1080/00397919008051599
TI - SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE
T2 - Synthetic Communications
AU - Schaus, John M.
AU - Huser, Diane L
AU - Titus, Robert D
PY - 1990
DA - 1990/12/01
PB - Taylor & Francis
SP - 3553-3562
IS - 22
VL - 20
SN - 0039-7911
SN - 1532-2432
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{1990_Schaus,
author = {John M. Schaus and Diane L Huser and Robert D Titus},
title = {SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE},
journal = {Synthetic Communications},
year = {1990},
volume = {20},
publisher = {Taylor & Francis},
month = {dec},
url = {https://doi.org/10.1080/00397919008051599},
number = {22},
pages = {3553--3562},
doi = {10.1080/00397919008051599}
}
Cite this
MLA
Copy
Schaus, John M., et al. “SYNTHESIS OF THE DOPAMINE AGONIST (-)-QUINPIROLE.” Synthetic Communications, vol. 20, no. 22, Dec. 1990, pp. 3553-3562. https://doi.org/10.1080/00397919008051599.