Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 233,120,640 papers from all fields of science
Search
Sign In
Create Free Account
Benzomorphans
Known as:
Benzomorphans [Chemical/Ingredient]
Morphine derivatives of the methanobenzazocine family that act as potent analgesics.
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
19 relations
Narrower (13)
BIII 277 CL
BIII 890 CL
Benzomorphan
GPA 1657
Expand
In Blood
agonists
antagonists & inhibitors
aspects of radiation effects
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Ethylene in organic synthesis: a new route to anticholenergic pyrrolidinoindolines, and other molecules with all carbon-quaternary centers via asymmetric hydrovinylation.
H. Lim
,
T. RajanBabu
Organic Letters
2011
Corpus ID: 207573217
The asymmetric hydrovinylation (1 mol % Ni-cat., 1 atm, ethylene, >98% ee) products from 1-methylenetetralines are readily…
Expand
2003
2003
Migratory hydroamination: a facile enantioselective synthesis of benzomorphans.
B. Trost
,
Weiping Tang
Journal of the American Chemical Society
2003
Corpus ID: 46626191
We describe a highly efficient, general strategy for the enantioselective synthesis of benzomorphans (45-46% overall yield from…
Expand
1995
1995
Effects of sigma receptor ligands on the extracellular concentration of dopamine in the striatum and prefrontal cortex of the rat.
G. Gudelsky
European Journal of Pharmacology
1995
Corpus ID: 20523414
The extracellular concentration of dopamine in the striatum and medial prefrontal cortex of the rat was determined following the…
Expand
1991
1991
Electrophilic gamma-lactone kappa-opioid receptor probes. Analogues of 2'-hydroxy-2-tetrahydrofurfuryl-5,9-dimethyl-6,7-benzomorphan diastereomers.
P. Klein
,
W. L. Nelson
Journal of Medicinal Chemistry
1991
Corpus ID: 19662050
Benzomorphans with an electrophilic group in the nitrogen substituent were prepared as potentially irreversible ligands for the…
Expand
1985
1985
The opioid receptors in the hamster vas deferens are of the delta-type.
A. Mcknight
,
A. Corbett
,
M. Marcoli
,
H. Kosterlitz
Neuropharmacology
1985
Corpus ID: 39298949
The motor responses of the isolated vas deferens of the hamster were unaffected by opioid-receptor agonists which are selective…
Expand
1978
1978
Benzomorphans. Structure of a position isomer.
N. Albertson
,
W. Michne
,
B. Tullar
Journal of Medicinal Chemistry
1978
Corpus ID: 12870355
May's benzomorphan synthesis leads not only to the alpha or cis isomer and the beta or trans isomer but also to a position isomer…
Expand
1977
1977
Application of the Free-Wilson technique to structurally related series of homologues. Quantitative structure-activity relationship studies of narcotic analgetics.
R. Katz
,
S. Osborne
,
F. Ionescu
Journal of Medicinal Chemistry
1977
Corpus ID: 36097811
A series of benzomorphans with ED50 values determined in vivo by the hot-plate method in mice is analyzed by the modified Free…
Expand
1975
1975
Synthesis and analgesic activities of 2,5-dimethyl-2'-hydroxy-9alpha- and -beta-propyl-6,7-benzomorphans.
K. Rice
,
A. Jacobson
,
E. May
Journal of Medicinal Chemistry
1975
Corpus ID: 33770919
The 2,5-dimethyl-2'-hydroxy-9alpha- and-beta-propyl-6,7-benzomorphans were synthesized from 4-methyl-3-propylpyridine in five…
Expand
1975
1975
Analgetic activity and in vitro binding constants of some N-alkyl-3-benzazocines.
M. E. Rogers
,
H. Ong
,
E. May
,
W. Klee
Journal of Medicinal Chemistry
1975
Corpus ID: 8650475
A homologous series of 3-alkyl-1,2,3,4,5,6-hexahydro-8-hydroxy-6-methyl-3-benzazocines (2) has been synthesized. Analgetic…
Expand
1967
1967
Benzomorphans. Optically Active and trans Isomers.
B. Tullar
,
L. Harris
,
+4 authors
N. Albertson
Journal of Medicinal Chemistry
1967
Corpus ID: 34772356
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE