Results 141 to 150 of about 4,192 (189)

The XylC-mediated aromatic metabolic network modulates the metabolic response of Pseudomonas aeruginosa to deltamethrin. [PDF]

BMC Microbiol
Wei X, Zhao X.
europepmc   +1 more source

<i>In vivo</i> selection of CMY-219 conferring resistance to ceftazidime-avibactam in an OXA-484-producing <i>E. coli</i> ST410. [PDF]

Antimicrob Agents Chemother
Jousset AB, Girlich D, Oueslati S, Birer A, Delaval A, Guyot C, Rezzoug I, Emeraud C, Naas T, Bonnin RA, Dortet L.   +10 more
europepmc   +1 more source

Photochemical thiocarbonyl difluoride generation enables azetidine synthesis. [PDF]

Nat Commun
Rodríguez RI, Paut J, Armellin G, Visentini S, Cormier G, Droghetti F, Natali M, Bortolus M, Pelosi G, Dell' Amico L.   +9 more
europepmc   +1 more source

Air-Stable Tetrazene Radical Cation Salts: Structural Requirements and Oxidation Catalysts. [PDF]

J Am Chem Soc
Oshiro A, Sasano Y, Saito S, Araki Y, Sugiyama S, Kwon E, Kajimoto S, Kuriyama Y, Yoshinaga S, Takahashi M, Sato K, Shida N, Ishigaki Y, Atobe M, Iwabuchi Y.   +14 more
europepmc   +1 more source

Asymmetric C-H Functionalization of <i>N</i>-Boc-2,5-dihydro-1<i>H</i>-pyrrole and Its Application as a Key Step in the Synthesis of (-)-Dragocin D. [PDF]

J Am Chem Soc
Nguyen TH, Shimabukuro K, Musaev DG, Bacsa J, Navarro A, Davies HML.   +5 more
europepmc   +1 more source

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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.
Regis Guillot, Jean Ollivier
exaly   +2 more sources

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
exaly   +3 more sources

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
exaly   +2 more sources

Piperidines and Azabicyclo Compounds. I. Via Michael Condensations

Journal of the American Chemical Society, 1950
Noel F Albertson
exaly   +2 more sources

A New Multicomponent Domino Reaction of 1,3-Dicarbonyl Compounds: One-Pot Access to Amino Azabicyclo[3.3.1]nonanones and 1,6-Hydro­naphthyridines

Synlett, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Celine Simon, Frederic Lieby‐Muller, Jean‐Francois Peyronel, Thierry Constantieux, Jean Rodriguez   +4 more
exaly   +2 more sources