✦ LIBER ✦

Synthesis and dopamine receptor binding of bridged tricyclic dopamine analogues

✍ Scribed by Haralambos E Katerinopoulous; Kyriaki Thermos; Demetrios K Vassilatis; David I Schuster

Publisher: Elsevier Science
Year: 1988
Tongue: French
Weight: 686 KB
Volume: 23
Category: Article
ISSN: 0223-5234
DOI: 10.1016/0223-5234(88)90215-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and dopaminergic properties of

Synthesis and dopaminergic properties of bridged tricyclic dopamine analogues

✍ Haralambos E Katerinopoulos; Kyriaki Thermos 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 307 KB

Synthesis of Piperazinylalkylisoxazoline

Synthesis of Piperazinylalkylisoxazoline Analogues and Their Binding Affinities for Dopamine Receptor Subtypes.

✍ Ji Young Jung; Sun Ho Jung; Hun Yeong Koh; Ae Nim Pae; Woo-Kyu Park; Jae Yang Ko 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 19 KB 👁 1 views

Phenylpiperazinylmethylheterocycle Deriv

Phenylpiperazinylmethylheterocycle Derivatives: Synthesis and Dopamine Receptor Binding Profiles

✍ Ashraf H. Abadi 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB

Synthesis and dopamine receptor binding

Synthesis and dopamine receptor binding affinity of 4H-thiochromenoapomorphines

✍ Attila Sipos; Miklós Tóth; Franziska K. U. Mueller; Jochen Lehmann; Sándor Berén 📂 Article 📅 2008 🏛 Springer Vienna 🌐 English ⚖ 362 KB

Azepino- and Diazepinoindoles: Synthesis

Azepino- and Diazepinoindoles: Synthesis and Dopamine Receptor Binding Profiles

✍ Johannes Kraxner; Harald H?bner; Peter Gmeiner 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 97 KB

Mapping the Catechol Binding Site in Dop

Mapping the Catechol Binding Site in Dopamine D1 Receptors: Synthesis and Evaluation of Two Parallel Series of Bicyclic Dopamine Analogues

✍ Dr. Lisa A. Bonner; Dr. Uros Laban; Benjamin R. Chemel; Jose I. Juncosa; Prof. M 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 596 KB

Scheme 2. Synthesis of 2 a-c, e. Reagents and conditions: a) BF 3 •Et 2 O, Et 3 SiH, CH 2 Cl 2 , 08C, 1 h; b) BF 3 •Et 2 O, allylTMS, CH 2 Cl 2 , 258C, 2 h; c) CyMgCl or AdMgBr, 0 8C, 1 h; d) Mitsunobu conditions, 25 8C, 2 h; e) H 2 , Pd/C, EtOH, 1 atm, 25 8C, 24 h. Scheme 3. Attempted synthesis of