Results 101 to 110 of about 3,581 (133)

<i>In vitro</i> evolution of durlobactam resistance in NDM-producing <i>Escherichia coli</i> due to a single mutation in <i>mrdA</i> encoding penicillin-binding protein 2. [PDF]

Antimicrob Agents Chemother
McElheny CL, Butcher EL, Kawai A, Shanks RMQ, Shields RK, Doi Y.   +5 more
europepmc   +1 more source

Straightforward Synthetic Approach to Aminoalcohols with 9-oxabicyclo[3.3.1]nonane or Cyclooctane Core via Nucleophilic Ring-Opening of Spirocyclic Bis(oxiranes). [PDF]

Molecules
Ryzhikova OV, Savchenkova DV, Kositov SV, Grishin YK, Maloshitskaya OA, Sedenkova KN, Averina EB.   +6 more
europepmc   +1 more source

[Studies on 1-azabicyclo compounds. IX. Condensation reaction of 3,4,6,7,8,9-hexahydro-2H-quinolizine with RNH 2 derivatives].

Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 1972
Y, Arata, S, Yoshifuji, T, Shioda
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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

Rh^I‐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, Youn K, Kang, Young Keun, Chung   +2 more
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New compounds: Preparation of Oxime Esters from 1-Azabicyclo[4.4.0]decane-4-one

Journal of Pharmaceutical Sciences, 1971
The synthesis of two new oxime esters is described. Preliminary results of pharmacological tests are also reported.
R V, Saenz, R A, Crochet
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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
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Azabicyclo[3.1.0]hexane-1-ols as frameworks for the asymmetric synthesis of biologically active compounds

Tetrahedron Letters, 2007
Azabicyclo[3.1.0]hexane-1-ols, easily obtained by Ti(IV)-mediated cyclopropanation of amino acid derivatives, constitute versatile, and unprecedented intermediates for the asymmetric synthesis of pharmacologically active products. Indeed, through selective rearrangement, these compounds undergo unusual ring cleavage to lead to pyrrolidinones.
Mouhamad Jida, Régis Guillot, Jean Ollivier   +2 more
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Iodofluorination of 2-azabicyclo[2.2.1]hept-5-en-3-ones and related compounds: Regio- and stereoselectivities

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, Yoshinori Ono, Chikara Kaneko   +2 more
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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