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Development of new radical cascades and multi-component reactions : application to the synthesis of nitrogen-containing heterocycles / / Marie-Helene Larraufie
| Development of new radical cascades and multi-component reactions : application to the synthesis of nitrogen-containing heterocycles / / Marie-Helene Larraufie |
| Autore | Larraufie Marie-Helene |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | Cham [Switzerland] : , : Springer, , 2014 |
| Descrizione fisica | 1 online resource (xxii, 326 pages) : illustrations (some color) |
| Disciplina | 547.590459 |
| Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
| Soggetto topico |
Heterocyclic compounds
Calcium cyanamide Quinazoline Guanidine |
| ISBN | 3-319-01324-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | INTRODUCTION -- PART A: N-ACYLCYANAMIDES AS NEW PARTNERS IN RADICAL CASCADES: SYNTHESIS OF POLYCYCLIC QUINAZOLINONES AND GUANIDINES -- THE CYANAMIDE MOIETY, SYNTHESIS AND REACTIVITY -- HOMOLYTIC AROMATIC SUBSTITUTIONS: STATE OF THE ART OF THE MECHANISTIC PROPOSALS -- RESULTS: DEVELOPMENTS OF NEW RADICAL CASCADES WITH N-ACYLCYANAMIDES -- OBJECTIVES OF THE PROJECT -- ADDITION OF ALKYL RADICALS -- ADDITION OF VINYL RADICALS TO N-ACYLCYANAMIDES -- ADDITION OF NITROGEN CENTERED RADICALS -- PREPARATION AND CYCLIZATION OF ALKYL PRECURSORS -- PREPARATION AND CYCLIZATION OF VINYL PRECURSORS -- PREPARATION AND CYCLIZATION OF AZIDE PRECURSORS -- PART B: VISIBLE-LIGHT PHOTOREDUCTIVE CATALYSIS FOR AN ECO-COMPATIBLE GENERATION OF RADICALS -- BIBLIOGRAPHICAL BACKGROUNDS: GENERATION OF RADICALS BY VISIBLE LIGHT PHOTOREDOX CATALYSIS -- PHOTOPHYSICAL PROPERTIES OF TRIS(BIPYRIDYL)RUTHENIUM(II) COMPLEXES -- STATE OF THE ART OF THE SUBSTRATES AMENABLE TO VISIBLE LIGHT PHOTOREDOX CATALYSIS -- RESULTS: VISIBLE LIGHT-INDUCED PHOTOREDUCTIVE GENERATION OF RADICALS FROM EPOXIDES AND AZIRIDINES -- EPOXIDES AS NEW SUBSTRATES FOR VISIBLE-LIGHT TRIGGERED GENERATION OF RADICALS -- SCOPE AND LIMITATIONS OF THE REDUCTIVE RING-OPENING METHODOLOGY -- UTILIZATION OF THE PHOTOGENERATED RADICALS IN CARBON-CARBON BOND FORMATIONS -- SUPPORTING INFORMATION -- GENERAL REMARKS -- GENERAL PROCEDURES -- EPOXIDE, AZIRIDINES AND CYCLOPROPANES PRECURSORS -- REDUCTIVE RING-OPENING PRODUCTS -- ALLYLATION PRODUCTS 246 -- PART C: NEW DEVELOPMENTS IN ARYL-ARYL COUPLINGS VIA PALLADIUM/NORBORNENE DUAL CATALYSIS: SYNTHESIS OF PHENANTHRIDINES AND PHENANTHRENES -- BIBLIOGRAPHICAL BACKGROUND: THE ORTHO EFFECT IN THE CATELLANI REACTION -- THE CATELLANI REACTION -- SYNTHETIC APPLICATIONS OF THE ORTHO EFFECT -- MECHANISTIC EXPLANATIONS FOR THE ORTHO EFFECT -- RESULTS: NEW PARTNERS FOR ORTHO-SUBSTITUTED ARYL IODIDES IN PALLADIUM/NORBORNENE COCATALYSIS -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND BROMOBENZYL AMINES: FIRST REPORTED CATELLANI SEQUENCE TERMINATED BY N-ARYL COUPLING WITH UNPROTECTED AMINES -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND 2-BROMOPHENYL ACETAMIDES: AN EXCEPTION TO THE ORTHO EFFECT -- SUPPORTING INFORMATION -- GENERAL REMARKS -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND BROMOBENZYL AMINES -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND 2-BROMOPHENYL ACETAMIDES. |
| Record Nr. | UNINA-9910298659303321 |
Larraufie Marie-Helene
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| Cham [Switzerland] : , : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Name reactions in heterocyclic chemistry [[electronic resource] /] / edited by Jie-Jack Li
| Name reactions in heterocyclic chemistry [[electronic resource] /] / edited by Jie-Jack Li |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2005 |
| Descrizione fisica | 1 online resource (579 p.) |
| Disciplina |
547.59
547.590459 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Comprehensive Name Reactions |
| Soggetto topico |
Heterocyclic chemistry
Chemical reactions |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-27303-8
9786610273034 0-470-35202-7 0-471-70414-8 0-471-70415-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions in Heterocyclic Chemistry; Table of Contents; Foreword; Preface; Acronyms and abbreviations; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Epoxides and Aziridines; 1.1 Corey-Chaykovsky reaction; 1.2 Darzens glycidic ester condensation; 1.3 Hoch-Campbell aziridine synthesis; 1.4 Jacobsen-Katsuki epoxidation; 1.5 Paterno-Buchi reaction; 1.6 Sharpless-Katsuki epoxidation; 1.7 Wenker aziridine synthesis; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Barton-Zard reaction; 2.2 Knorr and Paal-Knorr pyrrole syntheses
2.3 Hofmann-Loffler-Freytag reactionChapter 3 Indoles; 3.1 Bartoli indole synthesis; 3.2 Batcho-Leimgruber indole synthesis; 3.3 Bucherer carbazole synthesis; 3.4 Fischer indole synthesis; 3.5 Gassman indole synthesis; 3.6 Graebe-Ullman carbazole synthesis; 3.7 Hegedus indole synthesis; 3.8 Madelung indole synthesis; 3.9 Nenitzescu indole synthesis; 3.10 Reissert indole synthesis; Chapter 4 Furans; 4.1 Feist-Benary furan synthesis; 4.2 Paal-Knorr furan synthesis; Chapter 5 Thiophenes; 5.1 Fiesselmann thiophene synthesis; 5.2 Gewald aminothiophene synthesis 5.3 Hinsberg synthesis of thiophene derivatives5.4 Paal thiophene synthesis; Chapter 6 Oxazoles and Isoxazoles; 6.1 Claisen isoxazole synthesis; 6.2 Cornforth rearrangement; 6.3 Erlenmeyer-Plochl azlactone synthesis; 6.4 Fischer oxazole synthesis; 6.5 Meyers oxazoline method; 6.6 Robinson-Gabriel synthesis; 6.7 van Leusen oxazole Synthesis; Chapter 7 Other Five-Membered Heterocycles; 7.1 Auwers flavone synthesis; 7.2 Bucherer-Bergs reaction; 7.3 Cook-Heilbron 5-amino-thiazole synthesis; 7.4 Hurd-Mori 1,2,3-thiadiazole synthesis; 7.5 Knorr pyrazole synthesis; PART 3 SIX-MEMBERED HETEROCYCLES Chapter 8 Pyridines8.1 Preparation via condensation reactions; 8.1.1 Hantzsch (dihydro)-pyridine synthesis; 8.1.1.1 Description; 8.1.1.2 Historical perspective; 8.1.1.3 Mechanism; 8.1.1.4 Variations; 8.1.1.4.1 Guareschi-Thorpe pyridine synthesis; 8.1.1.4.2 Chichibabin (Tschitschibabin) pyridine synthesis; 8.1.1.4.3 Bohlmann-Rahtz pyridine synthesis; 8.1.1.4.4 Krohnke pyridine synthesis; 8.1.1.4.5 Petrenko-Kritschenko piperidone synthesis; 8.1.1.5 Improvements or modifications; 8.1.1.6 Experimental; 8.1.1.6.1 Three-component coupling; 8.1.1.6.2 Two-component coupling; 8.1.1.7 References 8.2 Preparation via cycloaddition reactions8.2.1 Boger reaction; 8.3 Preparation via rearrangement reactions; 8.3.1 Boekelheide reaction; 8.3.2 Ciamician-Dennstedt rearrangement; 8.4 Zincke reaction; Chapter 9 Quinolines and Isoquinolines; 9.1 Bischler-Napieralski reaction; 9.2 Camps quinoline synthesis; 9.3 Combes quinoline synthesis; 9.4 Conrad-Limpach reaction; 9.5 Doebner quinoline synthesis; 9.6 Friedlander synthesis; 9.7 Gabriel-Colman rearrangement; 9.8 Gould-Jacobs reaction; 9.9 Knorr quinoline synthesis; 9.10 Meth-Cohn quinoline synthesis; 9.11 Pfitzinger quinoline synthesis 9.12 Pictet-Gams isoquinoline synthesis |
| Record Nr. | UNINA-9910146073703321 |
| Hoboken, N.J., : Wiley-Interscience, c2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Name reactions in heterocyclic chemistry [[electronic resource] /] / edited by Jie-Jack Li
| Name reactions in heterocyclic chemistry [[electronic resource] /] / edited by Jie-Jack Li |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2005 |
| Descrizione fisica | 1 online resource (579 p.) |
| Disciplina |
547.59
547.590459 |
| Altri autori (Persone) | LiJie Jack |
| Collana | Comprehensive Name Reactions |
| Soggetto topico |
Heterocyclic chemistry
Chemical reactions |
| ISBN |
1-280-27303-8
9786610273034 0-470-35202-7 0-471-70414-8 0-471-70415-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Name Reactions in Heterocyclic Chemistry; Table of Contents; Foreword; Preface; Acronyms and abbreviations; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Epoxides and Aziridines; 1.1 Corey-Chaykovsky reaction; 1.2 Darzens glycidic ester condensation; 1.3 Hoch-Campbell aziridine synthesis; 1.4 Jacobsen-Katsuki epoxidation; 1.5 Paterno-Buchi reaction; 1.6 Sharpless-Katsuki epoxidation; 1.7 Wenker aziridine synthesis; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Barton-Zard reaction; 2.2 Knorr and Paal-Knorr pyrrole syntheses
2.3 Hofmann-Loffler-Freytag reactionChapter 3 Indoles; 3.1 Bartoli indole synthesis; 3.2 Batcho-Leimgruber indole synthesis; 3.3 Bucherer carbazole synthesis; 3.4 Fischer indole synthesis; 3.5 Gassman indole synthesis; 3.6 Graebe-Ullman carbazole synthesis; 3.7 Hegedus indole synthesis; 3.8 Madelung indole synthesis; 3.9 Nenitzescu indole synthesis; 3.10 Reissert indole synthesis; Chapter 4 Furans; 4.1 Feist-Benary furan synthesis; 4.2 Paal-Knorr furan synthesis; Chapter 5 Thiophenes; 5.1 Fiesselmann thiophene synthesis; 5.2 Gewald aminothiophene synthesis 5.3 Hinsberg synthesis of thiophene derivatives5.4 Paal thiophene synthesis; Chapter 6 Oxazoles and Isoxazoles; 6.1 Claisen isoxazole synthesis; 6.2 Cornforth rearrangement; 6.3 Erlenmeyer-Plochl azlactone synthesis; 6.4 Fischer oxazole synthesis; 6.5 Meyers oxazoline method; 6.6 Robinson-Gabriel synthesis; 6.7 van Leusen oxazole Synthesis; Chapter 7 Other Five-Membered Heterocycles; 7.1 Auwers flavone synthesis; 7.2 Bucherer-Bergs reaction; 7.3 Cook-Heilbron 5-amino-thiazole synthesis; 7.4 Hurd-Mori 1,2,3-thiadiazole synthesis; 7.5 Knorr pyrazole synthesis; PART 3 SIX-MEMBERED HETEROCYCLES Chapter 8 Pyridines8.1 Preparation via condensation reactions; 8.1.1 Hantzsch (dihydro)-pyridine synthesis; 8.1.1.1 Description; 8.1.1.2 Historical perspective; 8.1.1.3 Mechanism; 8.1.1.4 Variations; 8.1.1.4.1 Guareschi-Thorpe pyridine synthesis; 8.1.1.4.2 Chichibabin (Tschitschibabin) pyridine synthesis; 8.1.1.4.3 Bohlmann-Rahtz pyridine synthesis; 8.1.1.4.4 Krohnke pyridine synthesis; 8.1.1.4.5 Petrenko-Kritschenko piperidone synthesis; 8.1.1.5 Improvements or modifications; 8.1.1.6 Experimental; 8.1.1.6.1 Three-component coupling; 8.1.1.6.2 Two-component coupling; 8.1.1.7 References 8.2 Preparation via cycloaddition reactions8.2.1 Boger reaction; 8.3 Preparation via rearrangement reactions; 8.3.1 Boekelheide reaction; 8.3.2 Ciamician-Dennstedt rearrangement; 8.4 Zincke reaction; Chapter 9 Quinolines and Isoquinolines; 9.1 Bischler-Napieralski reaction; 9.2 Camps quinoline synthesis; 9.3 Combes quinoline synthesis; 9.4 Conrad-Limpach reaction; 9.5 Doebner quinoline synthesis; 9.6 Friedlander synthesis; 9.7 Gabriel-Colman rearrangement; 9.8 Gould-Jacobs reaction; 9.9 Knorr quinoline synthesis; 9.10 Meth-Cohn quinoline synthesis; 9.11 Pfitzinger quinoline synthesis 9.12 Pictet-Gams isoquinoline synthesis |
| Record Nr. | UNINA-9910830429203321 |
| Hoboken, N.J., : Wiley-Interscience, c2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Palladium in heterocyclic chemistry : a guide for the synthetic chemist / Jie Jack Li, Gordon W. Gribble
| Palladium in heterocyclic chemistry : a guide for the synthetic chemist / Jie Jack Li, Gordon W. Gribble |
| Autore | Li, Jie Jack |
| Pubbl/distr/stampa | Amsterdam : Pergamon, 2000 |
| Descrizione fisica | xviii, 413 p. : ill. ; 25 cm |
| Disciplina | 547.590459 |
| Altri autori (Persone) | Gribble, Gordon W. |
| Collana | Tetrahedron organic chemistry series ; 20 |
| Soggetto topico |
Heterocyclic compounds - Synthesis
Organopalladium compounds Palladium catalysts |
| ISBN |
0080437052
0080437044 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISALENTO-991000215329707536 |
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Li, Jie Jack
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| Amsterdam : Pergamon, 2000 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Salento | ||
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