✦ LIBER ✦

A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols

✍ Scribed by Bogdan A. Šolaja; Dragana R. Milić; Miroslav J. Gašić

Book ID: 103405968
Publisher: Elsevier Science
Year: 1996
Tongue: French
Weight: 192 KB
Volume: 37
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(96)00677-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Novel MCPBA Oxida

ChemInform Abstract: A Novel MCPBA Oxidation: p-Quinols and Epoxyquinols from Phenols.

✍ B. A. SOLAJA; D. R. MILIC; M. J. GASIC 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB

A Facile Microwave-Assisted Synthesis of

A Facile Microwave-Assisted Synthesis of p-Quinols by Lead(IV) Acetate Oxidation.

✍ Katalin Prokai-Tatrai; Nilka M. Rivera-Portalatin; Navin Rauniyar; Laszlo Prokai 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 22 KB 👁 1 views

ChemInform Abstract: Novel Heterocyclic

ChemInform Abstract: Novel Heterocyclic Betaines Relevant to the Mechanism of Tyrosinase-Catalyzed Oxidation of Phenols.

✍ J. CLEWS; C. J. COOKSEY; P. J. GARRATT; E. J. LAND; C. A. RAMSDEN; P. A. RILEY 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

Oxidation of 2,6-disubstituted phenols a

Oxidation of 2,6-disubstituted phenols as a route to 3,5,3′,5′-tetrasubstituted diphenoquinones and 4,4′-dihydroxydiphenyls

✍ M. Sh. Vakhitova; B. I. Pantukh; G. A. Tolstikov; O. P. Yablonskii; R. B. Svityc 📂 Article 📅 1987 🏛 Springer 🌐 English ⚖ 260 KB

Extra virgin olive oil phenols and marke

Extra virgin olive oil phenols and markers of oxidation in Greek smokers: a randomized cross-over study

✍ Moschandreas, J; Vissers, M N; Wiseman, S; van Putte, K P; Kafatos, A 📂 Article 📅 2002 🏛 Nature Publishing Group 🌐 English ⚖ 110 KB

Novel rearrangements of an N-oxide degra

Novel rearrangements of an N-oxide degradate formed from oxidation of a morpholine acetal substance P antagonist

✍ Zhao, Zhongxi Zack (author);Qin, Xue Zhi (author);Wu, Allen (author);Yuan, Yang 📂 Article 📅 2004 🏛 John Wiley and Sons Inc. 🌐 English ⚖ 88 KB

Compound 1 [5-[2(R)-[1(R)-(3,5-bistrifluoromethylphenyl) ethoxy]-3(s)-(4-fluorophenyl)morpholin-4-ylmethyl]-3h-[1,2,3] triazol-4-ylmethyl]dimethylamine represents a new class of potent, orally active substance P antagonists, which possess a characteristic structural feature-a cis-2-alkoxy-3-arylmorp