Results 151 to 160 of about 4,192 (189)

Synthesis of 3-azabicyclo[3.2.2]nonanes and their antiprotozoal activities

open access: yesBioorganic and Medicinal Chemistry Letters, 2015
Several bicyclic compounds, 3-azabicyclo[3.2.2]nonanes, have been prepared. The new compounds were tested for their activities against one strain of the causative organism of Malaria tropica, Plasmodium falciparum K1, which is resistant against ...
Werner Seebacher   +2 more
exaly   +2 more sources

5-Amino-azabicyclo[3.2.2] nonanes, a new class of compounds with antitrypanosomal and antimalarial activities

open access: yes, 2012
Plasmodium is one of the most deadly human parasites causing malaria. Four species of Plasmodium cause malaria, responsible for more than a million deaths per year. Two species of Trypanosome cause human African trypanosomiasis (HAT). Thirty six sub-Saharan countries are endemic of HAT bearing a death tool of about 30000.
Ahmad, Sarfraz
core   +3 more sources

RhI‐Catalyzed Cycloisomerization of Vinyl Bicyclopropyl Compounds to Azabicyclo[3.2.2]nona‐2,8‐dienes

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
openaire   +3 more sources

Azabicyclo Compounds—XI. A study of the fragmentation processes of quinuc‐lidine and some of its derivatives

Organic Mass Spectrometry, 1972
AbstractThe mass spectra of quinuclidine, all the ring position deuterated analogues and some methyl homologues have been measured. Plausible mechanistic interpretations of principal fragment ions are discussed, in the case of quinuclidine, with the help of deuteration in all the ring positions.
J. Paleček, J. Mitera
openaire   +1 more source

New Compounds: 3-[2-(2-Chloro-10-phenothiazinyl)ethyl]-3-azabicyclo[3.2.2]nonane

Journal of Pharmaceutical Sciences, 1967
The 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
openaire   +2 more sources

ChemInform Abstract: Azabicyclo[3.1.0]hexane‐1‐ols as Framework for the Asymmetric Synthesis of Biologically Active Compounds.

ChemInform, 2008
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Mouhamad Jida   +2 more
openaire   +1 more source

The Synthesis And Properties Of 9-azabicyclo (3.3.1)nonane Compounds.

1974
PhD ; Organic chemistry ; University of Michigan, Horace H. Rackham School of Graduate Studies ; http://deepblue.lib.umich.edu/bitstream/2027.42/191102/2/7510206 ...
openaire   +2 more sources

ChemInform Abstract: STUDIES ON 1‐AZABICYCLO COMPOUNDS PART 22, STEREOCHEMISTRY OF 9A‐SUBSTITUTED QUINOLIZIDINE METHIODIDES

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
openaire   +1 more source

ChemInform Abstract: A GENERAL SYNTHESIS OF DIBENZ(C,F)‐1‐AZABICYCLO(3.3.1)NONANE AND ITS RELATED COMPOUNDS

Chemischer Informationsdienst, 1978
AbstractAus den N,N‐Dibenzyl‐aminoacetaldehydacetalen (I) erhält man mit ′ Perchlorsäure die Cyclisierungsprodukte (II).
H. TAKAYAMA, M. TAKAMOTO, T. OKAMOTO
openaire   +1 more source

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