Results 121 to 130 of about 17,328 (234)
Stereoselective Synthesis of Cyclopropane Rings under Phase-Transfer-Catalyzed Conditions
Stereoselective Synthesis of Cyclopropane Rings under Phase-Transfer-Catalyzed ...
Kei-ichiro Hatano (3046020) +3 more
core +1 more source
Photoredox-catalyzed cyclopropanation of allenes towards vinyl-cyclopropanes
Visible-light photoredox-catalyzed regioselective radical-polar crossover cyclization (rRPCC) of terminal and internal allenes with carboxylic acids, access to functionalized vinyl cyclopropanes (VCPs).
Hui Xie, Yan Zhang, Bernhard Breit
openaire +2 more sources
Novel syntheses of γ-selenobutyrates from germinally diactivated cyclopropane derivatives
Cyclopropane carboxylic esters react with selenolates and lead to the corresponding cyclopropane carboxylic acids or to 4-seleno butyrates.
Krief, A., Trabelsi, M.
core
The molecular structures of 1-methyl-1-tert-butyl-cyclopropane and 1- methyl-l-iso-propyl-cyclopropane have been studied by gas-phase electron diffraction.
Marit Trætteberg +3 more
core
Cyclopropane Derivatives. I. Studies of the Photochemical and Thermal Chlorination of Cyclopropane
Gustavson has reported that the photochemical chlorination of cyclopropane gave 1, 1-dichlorocyclopropane and high-boiling compounds resulting from ring-opening reactions as the principal products.
Roberts, John D., Dirstine, Philip H.
core
Crystalline Silaspiropentane and Its Rearrangement to Silacyclobutane. [PDF]
Yang W, Stadler B, Crimmin MR.
europepmc +1 more source
New phenylcyclopropane-carbohydrazide furan derivatives with potent anticancer activity and EGFR inhibitory potential. [PDF]
Patagani S +6 more
europepmc +1 more source
Enflurane, isoflurane and cyclopropane.
The committee recommends the following health based occupational exposure limits: - enflurane: 20 ppm (153 mg/m3) TWA 8 h - isoflurane: 20 ppm (153 mg/m3) TWA 8 h. For cyclopropane no exposure limit can be recommended.
Maclaine Pont, M.A.
core
Discovery of dihydrospiro[cyclopropane-1,7'-pyrrolo[3,4-<i>d</i>]pyrimidine] derivatives as novel ATR inhibitors. [PDF]
Chen X +9 more
europepmc +1 more source

