The synthesis of (R)-(−) and (S)-(+)-hydroxysaclofen

Article Properties
  • Language
    English
  • Publication Date
    1995/10/01
  • Journal
  • Indian UGC (journal)
  • Refrences
    33
  • Rolf H. Prager
  • Karl Schafer
  • David P.G. Hamon
  • Ralph A. Massy-Westropp
Cite
H. Prager, Rolf, et al. “The Synthesis of (R)-(−) and (S)-(+)-Hydroxysaclofen”. Tetrahedron, vol. 51, no. 42, 1995, pp. 11465-72, https://doi.org/10.1016/0040-4020(95)00710-p.
H. Prager, R., Schafer, K., P.G. Hamon, D., & A. Massy-Westropp, R. (1995). The synthesis of (R)-(−) and (S)-(+)-hydroxysaclofen. Tetrahedron, 51(42), 11465-11472. https://doi.org/10.1016/0040-4020(95)00710-p
H. Prager, Rolf, Karl Schafer, David P.G. Hamon, and Ralph A. Massy-Westropp. “The Synthesis of (R)-(−) and (S)-(+)-Hydroxysaclofen”. Tetrahedron 51, no. 42 (1995): 11465-72. https://doi.org/10.1016/0040-4020(95)00710-p.
1.
H. Prager R, Schafer K, P.G. Hamon D, A. Massy-Westropp R. The synthesis of (R)-(−) and (S)-(+)-hydroxysaclofen. Tetrahedron. 1995;51(42):11465-72.
Refrences
Title Journal Journal Categories Citations Publication Date
10.1016/0960-894X(95)00016-M 1995
GABAA Receptor Agonists, Partial Agonists, and Antagonists. Design and Therapeutic Prospects Journal of Medicinal Chemistry
  • Medicine: Therapeutics. Pharmacology
  • Science: Chemistry: Analytical chemistry
  • Science: Chemistry
71 1994
The role of lysine 166 in the mechanism of mandelate racemase from Pseudomonas putida: Mechanistic and crystallographic evidence for stereospecific alkylation by (R)-.alpha.-phenylglycidate Biochemistry
  • Science: Biology (General)
  • Science: Biology (General)
  • Science: Chemistry: Organic chemistry: Biochemistry
  • Science: Biology (General)
  • Science: Chemistry: Organic chemistry: Biochemistry
72 1994
GABAB antagonists: Resolution, absolute stereochemistry, and pharmacology of (R)‐ and (S)‐phaclofen

Chirality
  • Medicine: Therapeutics. Pharmacology
  • Science: Chemistry: Analytical chemistry
  • Science: Chemistry: Organic chemistry
  • Medicine: Therapeutics. Pharmacology
  • Science: Chemistry: Analytical chemistry
  • Science: Chemistry
15 1994
10.1016/0021-9673(93)83055-W 1993
Refrences Analysis
The category Medicine: Internal medicine: Neurosciences. Biological psychiatry. Neuropsychiatry 12 is the most frequently represented among the references in this article. It primarily includes studies from Australian Journal of Chemistry and Journal of Neurochemistry. The chart below illustrates the number of referenced publications per year.
Refrences used by this article by year