<?xml version="1.0" encoding="UTF-8" ?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-01T20:47:25Z</responseDate><request metadataPrefix="oai_dc" identifier="oai:10442/0155" verb="GetRecord">https://phdtheses.ekt.gr/eadd_oai/request</request><GetRecord><record><header><identifier>oai:10442/0155</identifier><datestamp>2024-06-19T11:24:30Z</datestamp><setSpec>hdl_10442_2</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:description xmlns:lang="en">THE REACTION OF ALIPHATIC 1,3-DIOXIMES WITH LEAD TETRAACETATE (LTA)  RESULTED MAINLY IN PYRAZOLE- AND PYRAZOLINE - 1,2-DIOXIDES. THE EXACT TYPE  OF THE N-OXIDE FORMED, DEPENDS ON THE SUBSTITUENTS ON THE 2-POSITION OF  THE DIOXIME. FURTHERMORE, INFLUENCE IS ALSO EXERCISED BY ALKYL OR ARYL  GROUPS ADJACENT TO THE =NOH MOIETY. DEOXYGENATION OF THE ABOVE N- OXIDES WITH TRIETHYL PHOSPHITE PROCEEDSVERY DIFFICULTY TO THE PARENT  RING SYSTEM, WHEREAS DIELS-ALDER REACTION AND IRRADIATION WITH  MERCURY LAMP WERE UNSUCCESSFUL. FURTHERMORE, PRELIMINARY TESTSHAVE SHOWN PROMISING BIOLOGICAL ACTIVITY OF THESE COMPOUNDS. THE  OXIDATION WITH LTA OF SOME B-DIOXIMES WITH THE =NOH MOIETIES ATTACHED TO  THE CYCLOHEXANE RING LEADS TO PYRAZOLE AND PYRAZOLINE- 1,2 - DIOXIDES OR  TO GEM-NITROSO-ACETATES RATHER THAN THEIR ISOMERIC PYRAZOLE- 1,2 -  DIOXIDES IS PERSSUMABLY INFLUENCED BY THE CONFORMATIONAL EFFECTS OF  THE CYCLOHEXANE RING. TREATMENT OF THE GEM-NITROSOACETATES WITH  HYDROGEN PEROXIDE YIELDED THE CORRESPONDING NITRO COMPOUNDS,  WHEREAS WITH DILUTE HYDROCHLORIC ACID THE PARENT 1,3-DIKETONES WERE  REGENERATED. REACTION WITH ANILINE RESULTED MAINLY IN AZO- AND AZOXY -  BENZENE. FURTHERMORE, REACTION OF LTA WITH BIS-SCHIFT BASES, DERIVED  FROM THE CONDESATIONOF ETHYLENEDIAMINE WITH AROMATIC CARBONYLS,  GAVE HYDROLYSIS INSTEAD OF CYCLISATION PRODUCTS. FINALLY, REACTION OF  LTA WITH BIS-SCHIFT BASES OF DIACETYL ANDBENZIL YIELDED SUBSTITUTED  ACETANILIDE AND AZOBENZENE. PLANSIBLE MECHANISMS ARE PROPOSED FOR ALL  THE ABOVE CASES.</dc:description><dc:description xmlns:lang="el">ΣΤΗΝ ΔΙΑΤΡΙΒΗ ΑΥΤΗ ΜΕΛΕΤΑΤΑΙ ΔΙΕΞΟΔΙΚΑ Η ΟΞΕΙΔΩΣΗ Β-ΔΙΟΞΙΜΩΝ, ΚΑΘΩΣ ΚΑΙ  ΔΙΠΛΩΝΒΑΣΕΩΝ ΤΟΥ SCHIFT ΜΕ ΤΕΤΡΑΟΞΙΚΟ ΜΟΛΥΒΔΟ. ΕΠΙΣΗΣ ΜΕΛΕΤΑΤΑΙ Η  ΧΗΜΕΙΑ ΤΩΝ ΠΡΟΙΟΝΤΩΝ ΠΟΥ ΠΡΟΚΥΠΤΟΥΝ ΑΠΟ ΤΙΣ ΑΝΤΙΔΡΑΣΕΙΣ ΑΥΤΕΣ ΚΑΘΩΣ  ΚΑΙ Η ΠΡΑΚΤΙΚΗ ΕΦΑΡΜΟΓΗ ΤΟΥΣ.</dc:description><dc:title xmlns:lang="el">ΜΕΛΕΤΗ ΟΞΕΙΔΩΣΗΣ ΟΞΙΜΙΝΙΚΩΝ ΚΑΙ ΙΜΙΝΙΚΩΝ ΠΑΡΑΓΩΓΩΝ ΚΑΡΒΟΝΥΛΙΚΩΝ ΕΝΩΣΕΩΝ</dc:title><dc:title xmlns:lang="en">STUDIES ON THE OXIDATION OF B-DIOXIMES AND BIS-SCHIFF BASES</dc:title><dc:creator xmlns:lang="en">Kotali, Antigoni</dc:creator><dc:creator xmlns:lang="el">Κόταλη, Αντιγόνη</dc:creator><dc:date>1986</dc:date><dc:language>gre</dc:language><dc:subject xmlns:lang="el">Β-ΔΙΟΞΙΜΕΣ</dc:subject><dc:subject xmlns:lang="el">ΔΙΠΛΕΣ ΒΑΣΕΙΣ SCHIFF</dc:subject><dc:subject xmlns:lang="el">Οξείδωση</dc:subject><dc:subject xmlns:lang="el">Οργανική χημεία</dc:subject><dc:subject xmlns:lang="el">ΠΥΡΑΖΟΛΟ-1.2-ΔΙΟΞΕΙΔΙΑ</dc:subject><dc:subject xmlns:lang="el">Τετραοξικός μόλυβδος</dc:subject><dc:subject xmlns:lang="en">B-DIOXIMES</dc:subject><dc:subject xmlns:lang="en">BIS-SCHIFF BASES</dc:subject><dc:subject xmlns:lang="en">Lead tetraacetate</dc:subject><dc:subject xmlns:lang="en">Oxidation</dc:subject><dc:subject xmlns:lang="en">PYRAZOLE-1.2-DIOXIDES</dc:subject><dc:publisher xmlns:lang="en">Aristotle University Of Thessaloniki (AUTH)</dc:publisher><dc:publisher xmlns:lang="el">Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)</dc:publisher><dc:subject xmlns:lang="el">Επιστήμες Μηχανικού και Τεχνολογία</dc:subject><dc:subject xmlns:lang="el">Επιστήμη Χημικού Μηχανικού</dc:subject><dc:subject xmlns:lang="en">Engineering and Technology</dc:subject><dc:subject xmlns:lang="en">Chemical Engineering</dc:subject><dc:fathernamelatin>Dimitrios</dc:fathernamelatin><dc:identifier>10.12681/eadd/0155</dc:identifier><dc:identifier>http://hdl.handle.net/10442/hedi/0155</dc:identifier><dc:type>PhD Thesis</dc:type></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>