Reduction of Mercuric Salts by Dioxenes. R. K. Summerbell, George Herbert Kalb, Eric S. Graham, A. Louis Allred. J. Org. Chem. , 1962, 27 (12), pp 446...
Morris S. Kharasch, and Frederick W. Staveley ... Kwan , Paul S. Donnelly , Jonathan M. White , Allan J. Canty , Brian F. Yates , and Richard A. J. O'Hair.
The excess of oil is wiped off and the sheet allowed to dry in the air until ready to use,. Using paper thus prepared, as a negative, photographic copies can be.
Morris S. Kharasch, Frederick W. Staveley ... Hong-Yin Kwan , Paul S. Donnelly , Jonathan M. White , Allan J. Canty , Brian F. Yates , and Richard A. J. O'Hair.
Science in the US is built on immigrants. Will they keep coming?. Almost as soon as he started college, Morteza Khaledi knew he wanted to be a professor.
ARTICLES. Reduction of the Aqueous Mercuric Ion by Sulfite: UV Spectrum of HgSO3 and Its. Intramolecular Redox Reaction. Lisa Van Loon, Elizabeth Mader, ...
Potential Antipsoriatic Agents: Lapacho Compounds as Potent Inhibitors of HaCaT Cell Growth. Klaus M ller, Andreas Sellmer, and Wolfgang Wiegrebe.
Compound 6 was proven to be dimethyl adipate by comparison of its ir and nmr spectra with reference spectra. Saponification of. 0.0697 g of 6 uide supra gave ...
Apr 16, 1974 - Compound 6 was proven to be dimethyl adipate by comparison of its ir and nmr spectra with reference spectra. Saponification of. 0.0697 g of 6 ...
Aug 1, 1972 - Peter J. Wagner , Royal J. Truman , Alan E. Puchalski , Ronald. Wake. Journal of the American Chemical Society 1986 108 (24), 7727-7738.
Peter J. Wagner , Royal J. Truman , Alan E. Puchalski , Ronald. Wake. Journal of the American Chemical Society 1986 108 (24), 7727-7738. Abstract | PDF ...
DECEMBER, 1062
REDUCTION OF R~ERCURICSALTS BY Droxax~s
over. This latter process reduced the disulfide formed during the oxidation stage. The haloarylthiol wag extracted from the steam distillate with ether. The ether layer was dried over anhydrous sodium sulfate and the haloarylthiol recovered bv evaDoration of the ether and distillation. Table IV 1ist"s the haloarylthiola prepared by this method. Hdoaryl Disulfides.-The haloarylthiols obtained in the above process were all converted to their disulfides by the method described by Ritter and Sharpe.14 When the oxidative acid-cataIyzed-cleavage of the haloarylmercaptoacetio
446 1
acids w m carried out without using the steam distillation process the haloarylthiols produced were oxidized to their disulfides. Very high yields of haloaryl disulfides were obtained in all cases. Table V summarizes our results.
Acknowledgment.-We wish to thank the Directorsof ~ ~T~~and ~Chemical icompany, ~ Montreal, Canada, for permission to publish this work.
