{"id":{"repo_id":"greece","oai_identifier":"oai:10442/0719"},"canonical_url":"https://search.dev.ndltd.org/etd/greece/oai:10442/0719","repository":{"repo_id":"greece","name":"Greek National Archive of PhD Theses","base_url":"https://phdtheses.ekt.gr/eadd_oai/request"},"display":{"title":"ΣΥΝΘΕΣΗ ΚΑΙ ΜΕΛΕΤΗ 0-ΚΙΝΟΝΙΜΙΝΟ-, 0-ΚΙΝΟΝΟ-ΜΕΘΙΔΟ- ΚΑΙ Ο-ΚΙΝΟΝΙΜΙΝΟ- ΜΕΘΙΔΟ- ΠΑΡΑΓΩΓΩΝ ΤΗΣ 9, 10-ΦΑΙΝΑΝΘΡΕΝΟΚΙΝΟΝΗΣ ΚΑΙ ΤΗΣ 1, 2-ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗΣ","abstract":"10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH STABLE AND SEMISTABLE YLIDES AND O-QUINONE-METHIDE IMINES ARE ISOLATED. SOME OF THEM ARE THERMALLY CYCLIZED TO CONDENSED HETERCYCLIC COMPOUNDS . 10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH DIENOPHILES TO GIVE DIELS-ALDER PRODUCTS AND ALSO CONDENSED PYRIDINE DERIVATIVES . REACTIONS OF 10-METHOXY-IMINE-9-PHENANTHRENONE WITH METHYL- SUBSTITUTED AROMATIC COMPOUNDS LEAD TO THE FORMATION OF OXAZOLE- DERIVATIVES. 1,2-ACENAPHTHENEQUINONE-MONOXIME ALSO REACTS WITH STABLE AND SEMI-STABLE YLIDES AND THE RESPECTIVE O-QUINONE- METHIDE IMINES ARE FORMED. SEVERAL O-QUINONE-METHIDES OF 1,2- ACENAPHTHENEQUINONE REACT WITH NITROGEN COMPOUNDS TO GIVE PYRIDAZINE DERIVATIVES.","abstract_html":"10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH STABLE AND SEMISTABLE YLIDES AND O-QUINONE-METHIDE IMINES ARE ISOLATED. SOME OF THEM ARE THERMALLY CYCLIZED TO CONDENSED HETERCYCLIC COMPOUNDS . 10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH DIENOPHILES TO GIVE DIELS-ALDER PRODUCTS AND ALSO CONDENSED PYRIDINE DERIVATIVES . REACTIONS OF 10-METHOXY-IMINE-9-PHENANTHRENONE WITH METHYL- SUBSTITUTED AROMATIC COMPOUNDS LEAD TO THE FORMATION OF OXAZOLE- DERIVATIVES. 1,2-ACENAPHTHENEQUINONE-MONOXIME ALSO REACTS WITH STABLE AND SEMI-STABLE YLIDES AND THE RESPECTIVE O-QUINONE- METHIDE IMINES ARE FORMED. SEVERAL O-QUINONE-METHIDES OF 1,2- ACENAPHTHENEQUINONE REACT WITH NITROGEN COMPOUNDS TO GIVE PYRIDAZINE DERIVATIVES.","abstract_has_math":false,"creators":["Παπαγεωργίου, Γεώργιος"],"institution":"Aristotle University Of Thessaloniki (AUTH)","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1988,"date_issued":"1988","date_published":"1988","updated_at":"2026-07-24T02:25:24Z","subjects":["Αντιδράσεις Diels-Alder","ΑΝΤΙΔΡΑΣΕΙΣ WITTIG","Ο-ΚΙΝΟΝΙΜΙΝΕΣ","Ο-ΚΙΝΟΝΙΜΙΝΟ-ΜΕΘΙΔΙΑ","Ο-ΚΙΝΟΝΟΜΕΘΙΔΙΑ","ΠΑΡΑΓΩΓΑ 1,2-ΑΚΕΝΑΦΑΕΝΟΚΙΝΟΝΗΣ","ΠΑΡΑΓΩΓΑ 9,10-ΦΑΙΝΑΝΘΡΕΝΟΚΙΝΟΝΗΣ","ΣΥΝΘΕΣΗ ΟΞΑΖΟΛΙΩΝ","1,2-ACENAPHTHENE-QUINONEDERIVATIES","9,10-PHENANTHRENE-QUINONE DERIVATIES","Diels-Alder reactions","O-QUINONE-IMINES","O-QUINONE-METHIDE-IMINES","O-QUINONE-METHIDES","OXAZOLES SYNTHESIS","WITTIGREACTIONS","Φυσικές Επιστήμες","Χημεία","Natural Sciences","Chemical Sciences"],"languages":["gre"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["10.12681/eadd/0719"],"render_values":[{"text":"10.12681/eadd/0719","href":"https://doi.org/10.12681/eadd/0719","code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10442/hedi/0719","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Παπαγεωργίου, Γεώργιος"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["1988"]},{"key":"dc:publisher","label":"Institution","values":["Aristotle University Of Thessaloniki (AUTH)","Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)"]},{"key":"dc:type","label":"Dc Type","values":["PhD Thesis"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Αντιδράσεις Diels-Alder","ΑΝΤΙΔΡΑΣΕΙΣ WITTIG","Ο-ΚΙΝΟΝΙΜΙΝΕΣ","Ο-ΚΙΝΟΝΙΜΙΝΟ-ΜΕΘΙΔΙΑ","Ο-ΚΙΝΟΝΟΜΕΘΙΔΙΑ","ΠΑΡΑΓΩΓΑ 1,2-ΑΚΕΝΑΦΑΕΝΟΚΙΝΟΝΗΣ","ΠΑΡΑΓΩΓΑ 9,10-ΦΑΙΝΑΝΘΡΕΝΟΚΙΝΟΝΗΣ","ΣΥΝΘΕΣΗ ΟΞΑΖΟΛΙΩΝ","1,2-ACENAPHTHENE-QUINONEDERIVATIES","9,10-PHENANTHRENE-QUINONE DERIVATIES","Diels-Alder reactions","O-QUINONE-IMINES","O-QUINONE-METHIDE-IMINES","O-QUINONE-METHIDES","OXAZOLES SYNTHESIS","WITTIGREACTIONS","Φυσικές Επιστήμες","Χημεία","Natural Sciences","Chemical Sciences"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["gre"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["10.12681/eadd/0719","http://hdl.handle.net/10442/hedi/0719"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH STABLE AND SEMISTABLE YLIDES AND O-QUINONE-METHIDE IMINES ARE ISOLATED. SOME OF THEM ARE THERMALLY CYCLIZED TO CONDENSED HETERCYCLIC COMPOUNDS . 10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH DIENOPHILES TO GIVE DIELS-ALDER PRODUCTS AND ALSO CONDENSED PYRIDINE DERIVATIVES . REACTIONS OF 10-METHOXY-IMINE-9-PHENANTHRENONE WITH METHYL- SUBSTITUTED AROMATIC COMPOUNDS LEAD TO THE FORMATION OF OXAZOLE- DERIVATIVES. 1,2-ACENAPHTHENEQUINONE-MONOXIME ALSO REACTS WITH STABLE AND SEMI-STABLE YLIDES AND THE RESPECTIVE O-QUINONE- METHIDE IMINES ARE FORMED. SEVERAL O-QUINONE-METHIDES OF 1,2- ACENAPHTHENEQUINONE REACT WITH NITROGEN COMPOUNDS TO GIVE PYRIDAZINE DERIVATIVES.","ΣΤΗ ΔΙΑΤΡΙΒΗ ΑΥΤΗ ΓΙΝΕΤΑΙ ΜΕΛΕΤΗ ΑΝΤΙΔΡΑΣΕΩΝ WITTIG ΤΗΣ 10- ΜΕΘΟΞΥΙΜΙΝΟ-9-ΦΑΙΝΑΝΘΡΟΝΗΣ ΜΕ ΔΙΑΦΟΡΑ ΣΤΑΘΕΡΑ ΚΑΙ ΗΜΙΣΤΑΘΕΡΑ ΥΛΙΔΙΑ ΤΟΥ ΦΩΣΦΟΡΟΥ ΑΠ'ΟΠΟΥ ΑΠΟΜΟΝΩΝΟΝΤΑΙ ΤΑ ΑΝΤΙΣΤΟΙΧΑ Ο- ΚΙΝΟΝΙΜΙΝΟ- ΜΕΘΙΔΙΑ, ΟΡΙΣΜΕΝΑ ΑΠΟ ΤΑ ΟΠΟΙΑ ΚΥΚΛΟΠΟΙΟΥΝΤΑΙΣΤΗ ΣΥΝΕΧΕΙΑ ΠΡΟΣ ΠΟΛΥΣΥΜΠΥΚΝΩΜΕΝΑ ΠΥΡΙΔΙΝΙΚΑ ΠΑΡΑΓΩΓΑ. ΑΝΤΙΔΡΑΣΕΙΣ DIELS-ALDER ΤΗΣ 10-ΜΕΘΟΞΥΙΜΙΝΟ-9-ΦΑΙΝΑΝΘΡΟΝΗΣ ΚΑΘΩΣ ΚΑΙ ΑΝΤΙΣΤΟΙΧΩΝ ΚΙΝΟΜΙΝΟ- ΜΕΘΙΔΙΩΝ ΤΟΥΣ ΜΕ ΔΙΕΝΟΦΙΛΟ ΑΝΤΙΔΡΑΣΤΗΡΙΑ ΚΑΤΑΛΗΓΟΥΝ ΣΕ ΕΤΕΡΟΚΥΚΛΙΚΑ ΠΟΛΥΣΜΠΥΚΝΩΜΕΝΑ ΠΑΡΑΓΩΓΑ. ΑΝΤΙΔΡΑΣΕΙΣ ΤΗΣ 10- ΜΕΘΟΞΥΙΜΙΝΟ-9-ΦΑΙΝΑΝΘΡΟΝΗΣ ΜΕ ΜΕΘΥΛΟ-ΥΠΟΚΑΤΕΣΤΗΜΕΝΑ ΑΡΩΜΑΤΙΚΑ ΣΥΣΤΗΜΑΤΑ ΕΧΟΥΝ ΣΑΝ ΑΠΟΤΕΛΕΣΜΑ ΤΗ ΣΥΝΘΕΣΗ ΕΞΑΖΟΛΙΩΝ. Η ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗ ΑΝΤΙΔΡΑ ΕΠΙΣΗΣ ΜΕ ΣΤΑΘΕΡΑ ΚΑΙ ΗΜΙΣΤΑΘΕΡΑ ΥΛΙΔΙΑ ΤΟΥ ΦΩΣΦΟΡΟΥ ΔΙΝΟΝΤΑΣ ΚΥΡΙΩΣ ΤΑΑΝΤΙΣΤΟΙΧΑ Ο-ΚΙΝΟΝΙΜΙΝΟΜΕΘΙΔΙΑ ΔΙΑΦΟΡΑ Ο-ΚΙΝΟΝΟΜΕΘΙΔΙΑ ΤΗΣ 1,2-ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗΣ ΑΝΤΙΔΡΟΥΝ ΜΕ ΑΖΩΤΟΥΧΕΣ ΕΝΩΣΕΙΣ ΚΑΤΑΛΗΓΟΝΤΑΣ ΣΕ ΕΝΔΙΑΦΕΡΟΝΤΑ ΠΥΡΙΔΑΖΙΝΙΚΑ ΠΑΡΑΓΩΓΑ."]},{"key":"dc:title","label":"Title","values":["ΣΥΝΘΕΣΗ ΚΑΙ ΜΕΛΕΤΗ 0-ΚΙΝΟΝΙΜΙΝΟ-, 0-ΚΙΝΟΝΟ-ΜΕΘΙΔΟ- ΚΑΙ Ο-ΚΙΝΟΝΙΜΙΝΟ- ΜΕΘΙΔΟ- ΠΑΡΑΓΩΓΩΝ ΤΗΣ 9, 10-ΦΑΙΝΑΝΘΡΕΝΟΚΙΝΟΝΗΣ ΚΑΙ ΤΗΣ 1, 2-ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗΣ","SYNTHESIS AND STUDY OF O-QUINONE IMINES, O-QUINONE METHIDES, O-QUINONE METHIDE IMINES DERIVATIVES OF 9, 10-PHENANTHRENE QUINONE AND 1, 2-ACENAPHTHENE-QUINONE"]}]}],"canonical_facts":{"dc:creator":["Παπαγεωργίου, Γεώργιος"],"dc:date":["1988"],"dc:description":["10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH STABLE AND SEMISTABLE YLIDES AND O-QUINONE-METHIDE IMINES ARE ISOLATED. SOME OF THEM ARE THERMALLY CYCLIZED TO CONDENSED HETERCYCLIC COMPOUNDS . 10-METHOXY-IMINE-9-PHENANTHRENONE REACTS WITH DIENOPHILES TO GIVE DIELS-ALDER PRODUCTS AND ALSO CONDENSED PYRIDINE DERIVATIVES . REACTIONS OF 10-METHOXY-IMINE-9-PHENANTHRENONE WITH METHYL- SUBSTITUTED AROMATIC COMPOUNDS LEAD TO THE FORMATION OF OXAZOLE- DERIVATIVES. 1,2-ACENAPHTHENEQUINONE-MONOXIME ALSO REACTS WITH STABLE AND SEMI-STABLE YLIDES AND THE RESPECTIVE O-QUINONE- METHIDE IMINES ARE FORMED. SEVERAL O-QUINONE-METHIDES OF 1,2- ACENAPHTHENEQUINONE REACT WITH NITROGEN COMPOUNDS TO GIVE PYRIDAZINE DERIVATIVES.","ΣΤΗ ΔΙΑΤΡΙΒΗ ΑΥΤΗ ΓΙΝΕΤΑΙ ΜΕΛΕΤΗ ΑΝΤΙΔΡΑΣΕΩΝ WITTIG ΤΗΣ 10- ΜΕΘΟΞΥΙΜΙΝΟ-9-ΦΑΙΝΑΝΘΡΟΝΗΣ ΜΕ ΔΙΑΦΟΡΑ ΣΤΑΘΕΡΑ ΚΑΙ ΗΜΙΣΤΑΘΕΡΑ ΥΛΙΔΙΑ ΤΟΥ ΦΩΣΦΟΡΟΥ ΑΠ'ΟΠΟΥ ΑΠΟΜΟΝΩΝΟΝΤΑΙ ΤΑ ΑΝΤΙΣΤΟΙΧΑ Ο- ΚΙΝΟΝΙΜΙΝΟ- ΜΕΘΙΔΙΑ, ΟΡΙΣΜΕΝΑ ΑΠΟ ΤΑ ΟΠΟΙΑ ΚΥΚΛΟΠΟΙΟΥΝΤΑΙΣΤΗ ΣΥΝΕΧΕΙΑ ΠΡΟΣ ΠΟΛΥΣΥΜΠΥΚΝΩΜΕΝΑ ΠΥΡΙΔΙΝΙΚΑ ΠΑΡΑΓΩΓΑ. ΑΝΤΙΔΡΑΣΕΙΣ DIELS-ALDER ΤΗΣ 10-ΜΕΘΟΞΥΙΜΙΝΟ-9-ΦΑΙΝΑΝΘΡΟΝΗΣ ΚΑΘΩΣ ΚΑΙ ΑΝΤΙΣΤΟΙΧΩΝ ΚΙΝΟΜΙΝΟ- ΜΕΘΙΔΙΩΝ ΤΟΥΣ ΜΕ ΔΙΕΝΟΦΙΛΟ ΑΝΤΙΔΡΑΣΤΗΡΙΑ ΚΑΤΑΛΗΓΟΥΝ ΣΕ ΕΤΕΡΟΚΥΚΛΙΚΑ ΠΟΛΥΣΜΠΥΚΝΩΜΕΝΑ ΠΑΡΑΓΩΓΑ. ΑΝΤΙΔΡΑΣΕΙΣ ΤΗΣ 10- ΜΕΘΟΞΥΙΜΙΝΟ-9-ΦΑΙΝΑΝΘΡΟΝΗΣ ΜΕ ΜΕΘΥΛΟ-ΥΠΟΚΑΤΕΣΤΗΜΕΝΑ ΑΡΩΜΑΤΙΚΑ ΣΥΣΤΗΜΑΤΑ ΕΧΟΥΝ ΣΑΝ ΑΠΟΤΕΛΕΣΜΑ ΤΗ ΣΥΝΘΕΣΗ ΕΞΑΖΟΛΙΩΝ. Η ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗ ΑΝΤΙΔΡΑ ΕΠΙΣΗΣ ΜΕ ΣΤΑΘΕΡΑ ΚΑΙ ΗΜΙΣΤΑΘΕΡΑ ΥΛΙΔΙΑ ΤΟΥ ΦΩΣΦΟΡΟΥ ΔΙΝΟΝΤΑΣ ΚΥΡΙΩΣ ΤΑΑΝΤΙΣΤΟΙΧΑ Ο-ΚΙΝΟΝΙΜΙΝΟΜΕΘΙΔΙΑ ΔΙΑΦΟΡΑ Ο-ΚΙΝΟΝΟΜΕΘΙΔΙΑ ΤΗΣ 1,2-ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗΣ ΑΝΤΙΔΡΟΥΝ ΜΕ ΑΖΩΤΟΥΧΕΣ ΕΝΩΣΕΙΣ ΚΑΤΑΛΗΓΟΝΤΑΣ ΣΕ ΕΝΔΙΑΦΕΡΟΝΤΑ ΠΥΡΙΔΑΖΙΝΙΚΑ ΠΑΡΑΓΩΓΑ."],"dc:identifier":["10.12681/eadd/0719","http://hdl.handle.net/10442/hedi/0719"],"dc:language":["gre"],"dc:publisher":["Aristotle University Of Thessaloniki (AUTH)","Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)"],"dc:subject":["Αντιδράσεις Diels-Alder","ΑΝΤΙΔΡΑΣΕΙΣ WITTIG","Ο-ΚΙΝΟΝΙΜΙΝΕΣ","Ο-ΚΙΝΟΝΙΜΙΝΟ-ΜΕΘΙΔΙΑ","Ο-ΚΙΝΟΝΟΜΕΘΙΔΙΑ","ΠΑΡΑΓΩΓΑ 1,2-ΑΚΕΝΑΦΑΕΝΟΚΙΝΟΝΗΣ","ΠΑΡΑΓΩΓΑ 9,10-ΦΑΙΝΑΝΘΡΕΝΟΚΙΝΟΝΗΣ","ΣΥΝΘΕΣΗ ΟΞΑΖΟΛΙΩΝ","1,2-ACENAPHTHENE-QUINONEDERIVATIES","9,10-PHENANTHRENE-QUINONE DERIVATIES","Diels-Alder reactions","O-QUINONE-IMINES","O-QUINONE-METHIDE-IMINES","O-QUINONE-METHIDES","OXAZOLES SYNTHESIS","WITTIGREACTIONS","Φυσικές Επιστήμες","Χημεία","Natural Sciences","Chemical Sciences"],"dc:title":["ΣΥΝΘΕΣΗ ΚΑΙ ΜΕΛΕΤΗ 0-ΚΙΝΟΝΙΜΙΝΟ-, 0-ΚΙΝΟΝΟ-ΜΕΘΙΔΟ- ΚΑΙ Ο-ΚΙΝΟΝΙΜΙΝΟ- ΜΕΘΙΔΟ- ΠΑΡΑΓΩΓΩΝ ΤΗΣ 9, 10-ΦΑΙΝΑΝΘΡΕΝΟΚΙΝΟΝΗΣ ΚΑΙ ΤΗΣ 1, 2-ΑΚΕΝΑΦΘΕΝΟΚΙΝΟΝΗΣ","SYNTHESIS AND STUDY OF O-QUINONE IMINES, O-QUINONE METHIDES, O-QUINONE METHIDE IMINES DERIVATIVES OF 9, 10-PHENANTHRENE QUINONE AND 1, 2-ACENAPHTHENE-QUINONE"],"dc:type":["PhD Thesis"]},"updated_at":"2026-07-24T02:25:24Z"}