✦ LIBER ✦

A new oxidative cleavage of α-diketones and o-quinones by an oxygen adduct of cobaltocene

✍ Scribed by H. Kojima; S. Takahashi; N. Hagihara

Publisher: Elsevier Science
Year: 1973
Tongue: French
Weight: 133 KB
Volume: 14
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)96101-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A New, Modulated, O

ChemInform Abstract: A New, Modulated, Oxidative Ring Cleavage of α-Nitrocycloalkanones by Oxone®: Synthesis of α,ω-Dicarboxylic Acids and α,ω-Dicarboxylic Acid Monomethyl Esters.

✍ R. BALLINI; M. CURINI; F. EPIFANO; M. C. MARCOTULLIO; O. ROSATI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

ChemInform Abstract: Photochemical Behav

ChemInform Abstract: Photochemical Behavior of α-Diketones on a Silica Gel Surface: A Novel Photoreaction by Intramolecular Trapping of an Excited Ketone Carbonyl Oxygen by an Aryl Group.

✍ T. HASEGAWA; M. IMADA; Y. IMASE; Y. YAMAZAKI; M. YOSHIOKA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

A new synthesis ofortho-Quinones by tran

A new synthesis ofortho-Quinones by transition-metal-mediated oxygenation of phenols withtert-butylhydroperoxide and the mimoun oxodiperoxo molybdenum complex [Mo(O2)2O] · Py · HMPT

✍ Krohn, Karsten ;Rieger, Hagen ;Khanbabaee, Karamali 📂 Article 📅 1989 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 835 KB

A specific oxygenation of phenols to ortho-quinones can be effected by a combination of the transition metal complexes Ti(OiPr)4, Vqacack, Zr(acac),, Zr(0nPrh and tert-butylhydro-B 2323 Eine nene ortbChinon-Synthese dmcb Oxygenhmg vott Wen o h mit den systemen tert-Butyihydroperoxid/ObergnngsmetaU-K

ChemInform Abstract: Substituent-Dictate

ChemInform Abstract: Substituent-Dictated Partitioning of Intermediates on the Sulfide Singlet Oxygen Reaction Surface. A New Mechanism for Oxidative C—S Bond Cleavage in α-Hydroperoxy Sulfides.

✍ Alexei Toutchkine; David Aebisher; Edward L. Clennan 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Tentative partial oxidation of the nicke

Tentative partial oxidation of the nickel(II) potassium-dithiooxalato complex: Existence of iodine an adduct K2Ni(S2C2O2)2I in solution and crystal structure of a new polymorphic form of K2Ni(S2C2O2)2 (‘black’ form)

✍ A. Gleizes; F. Clery; M.F. Bruniquel; P. Cassoux 📂 Article 📅 1979 🏛 Elsevier Science 🌐 English ⚖ 709 KB

## Tentative partial oxidation of 'red' nickel(R) potassiumdithiooxalate K2Ni(S2C,0,), by iodine results in a K2Ni(S&0,)J adduct. This adduct was identified in solution but could not be isolated in the solid state. Operating with KzCrzO, surprisingly leads to a polymorphic 'black' form of KaNi(S,C,-