Explore: Tetrahydronaphthalenes
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Books Results
Source: The Open Library
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1Brain 5HT 1A Receptors
By Colin T. Dourish

“Brain 5HT 1A Receptors” Metadata:
- Title: Brain 5HT 1A Receptors
- Author: Colin T. Dourish
- Language: English
- Number of Pages: Median: 306
- Publisher: ➤ VCH - Wiley-VCH - Ellis Horwood - Distribution, USA and Canada, VCH Publishers - Vch Pub
- Publish Date: 1987 - 1988
- Publish Location: ➤ New York, NY, USA - Weinheim, Federal Republic of Germany - Weinheim - Chichester, England - Chichester
“Brain 5HT 1A Receptors” Subjects and Themes:
- Subjects: ➤ Brain chemistry - Neural receptors - Neurotransmitter receptors - Serotonin - Receptors - Behavior - Drug effects - Brain Chemistry - Serotonin Receptors - Metabolism - Tetrahydronaphthalenes - Pharmacodynamics - Pharmacology
Edition Identifiers:
- The Open Library ID: OL8252162M - OL12765815M - OL21840038M - OL2393114M
- Online Computer Library Center (OCLC) ID: 16684038
- Library of Congress Control Number (LCCN): 87022644
- All ISBNs: 3527265538 - 9780895735751 - 089573575X - 9783527265534
Access and General Info:
- First Year Published: 1987
- Is Full Text Available: No
- Is The Book Public: No
- Access Status: No_ebook
Online Access
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Wiki
Source: Wikipedia
Wikipedia Results
Search Results from Wikipedia
Decalin
Decalin (decahydronaphthalene, also known as bicyclo[4.4.0]decane and sometimes decaline), a bicyclic organic compound, is an industrial solvent. A colorless
Tetralin
Tetralin (1,2,3,4-tetrahydronaphthalene) is a hydrocarbon having the chemical formula C10H12. It is a partially hydrogenated derivative of naphthalene
Diphenhydramine
field analysis studies of 2-dimethylamino-5-(6)-phenyl-1,2,3,4-tetrahydronaphthalenes". Bioorganic & Medicinal Chemistry. 14 (19): 6640–58. doi:10.1016/j
Amitriptyline
field analysis studies of 2-dimethylamino-5-(6)-phenyl-1,2,3,4-tetrahydronaphthalenes". Bioorganic & Medicinal Chemistry. 14 (19): 6640–6658. doi:10.1016/j
1-Tetralone
medicine. As already described in 1933 by Heinrich Hock, 1,2,3,4-tetrahydronaphthalene tends to autoxidize and gradually forms the 1-hydroperoxide with
Stereoselectivity
Friedel-Crafts Cyclization Reactions to 2-Substituted 1-Phenyl-1,2,3,4-tetrahydronaphthalenes Friedrich Mühlthau, Thorsten Bach Synthesis 2005: 3428-3436 doi:10
1-Aminotetralin
1-Aminotetralin (1-AT), also known as 1-amino-1,2,3,4-tetrahydronaphthalene, is a chemical compound and one of the possible positional isomers of aminotetralin
Enol
Naphthalene-1,4-diol exists in observable equilibrium with the diketone tetrahydronaphthalene-1,4-dione. Keto–enol tautomerism is important in several areas of
Naphthalene
high pressure in the presence of metal catalysts to give 1,2,3,4-tetrahydronaphthalene(C 10H 12), also known as tetralin. Further hydrogenation yields
Nortriptyline
field analysis studies of 2-dimethylamino-5-(6)-phenyl-1,2,3,4-tetrahydronaphthalenes". Bioorg. Med. Chem. 14 (19): 6640–58. doi:10.1016/j.bmc.2006.05