Results 181 to 190 of about 7,278 (228)
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Piperidines and Azabicyclo Compounds. I. Via Michael Condensations
Journal of the American Chemical Society, 1950openaire +3 more sources
Carbon-13 NMR studies of 9-methyl-9-azabicyclo[3.3.1]nonane and related compounds
Journal of the American Chemical Society, 1976S. F. Nelsen +3 more
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Reductive Cyclization. A General Method for the Synthesis of 1-Azabicyclo Compounds1,2
Nelson J. Leonard, William E. Goode
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New Compounds: 3-[2-(2-Chloro-10-phenothiazinyl)ethyl]-3-azabicyclo[3.2.2]nonane
Journal of Pharmaceutical Sciences, 1967The synthesis of 3-[2-(2-chloro-10-pheno-thiazinyl)ethyl] - 3 - azabicyclo[3.2.2]non-ane is reported; the pharmacological evaluation of this agent, an analog of promethazine, has not yet been reported.
W T, King, C H, Bruening, W L, Nobles
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Chemistry – A European Journal, 2010
AbstractNitrogen‐containing heterobicycles can be synthesized from vinyl bicyclopropyl derivatives in the presence of a Rh(I) catalyst.
Sun Young, Kim +2 more
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AbstractNitrogen‐containing heterobicycles can be synthesized from vinyl bicyclopropyl derivatives in the presence of a Rh(I) catalyst.
Sun Young, Kim +2 more
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Chemischer Informationsdienst, 1975
AbstractDie Chinolizidine (I) reagieren mit Methyljodid jeweils zu einem Gemisch der cisund trans‐Verbindungen (II) und (III).
Y. ARATA, T. AOKI, M. HANAOKA, M. KAMEI
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AbstractDie Chinolizidine (I) reagieren mit Methyljodid jeweils zu einem Gemisch der cisund trans‐Verbindungen (II) und (III).
Y. ARATA, T. AOKI, M. HANAOKA, M. KAMEI
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Tetrahedron Letters, 1995
Abstract Iodofluorination of two types of allylic compounds with an amino group at the allylic position (2-azabicyclo[2.2.1]heptenes and cyclopentenylamines) was examined and the regio- and stereoselectivities have been clarified.
Akemi Toyota +2 more
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Abstract Iodofluorination of two types of allylic compounds with an amino group at the allylic position (2-azabicyclo[2.2.1]heptenes and cyclopentenylamines) was examined and the regio- and stereoselectivities have been clarified.
Akemi Toyota +2 more
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Tetrahedron, 1993
Abstract Morpholino-chlorotetrahydro-N-methyl-pyridine 4 reacted with Grignard reagents 5 or diorganyl-magnesium compounds 6 to give a mixture of azabicyclo[3.1.0]hexane diastereomers 10 and 11 besides the monocyclic ketones 12. The latter were obtained as the sole products from chloroenamine 4 and dimethylzinc 7a or lithium dimethylcopper 8a ...
Volker Butz, Elmar Vilsmaier
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Abstract Morpholino-chlorotetrahydro-N-methyl-pyridine 4 reacted with Grignard reagents 5 or diorganyl-magnesium compounds 6 to give a mixture of azabicyclo[3.1.0]hexane diastereomers 10 and 11 besides the monocyclic ketones 12. The latter were obtained as the sole products from chloroenamine 4 and dimethylzinc 7a or lithium dimethylcopper 8a ...
Volker Butz, Elmar Vilsmaier
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