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Biblioteca

MARC Lista (tabellare)
Asymmetric synthesis of natural products / Ari Koskinen
Asymmetric synthesis of natural products / Ari Koskinen
Autore Koskinen, Ari
Pubbl/distr/stampa Chichester : John Wiley & Sons, c1993
Descrizione fisica xiii, 234 p. : ill. ; 25 cm
Disciplina 547.7
Soggetto topico Asymmetry (Chemistry)
Natural products - Synthesis
ISBN 0471938483
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991003424229707536
Koskinen, Ari  
Chichester : John Wiley & Sons, c1993
Materiale a stampa
Lo trovi qui: Univ. del Salento
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Efficiency in natural product total synthesis / / edited by Pei-Qiang Huang, Zhu-Jun Yao, Richard P. Hsung
Efficiency in natural product total synthesis / / edited by Pei-Qiang Huang, Zhu-Jun Yao, Richard P. Hsung
Edizione [First edition.]
Pubbl/distr/stampa Hoboken, NJ : , : Wiley, , 2018
Descrizione fisica 1 online resource (514 pages)
Disciplina 547/.2
Soggetto topico Natural products - Synthesis
Organic compounds - Synthesis
ISBN 1-118-94021-0
1-118-94020-2
1-118-94022-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910555060303321
Hoboken, NJ : , : Wiley, , 2018
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Efficiency in natural product total synthesis / / edited by Pei-Qiang Huang, Zhu-Jun Yao, Richard P. Hsung
Efficiency in natural product total synthesis / / edited by Pei-Qiang Huang, Zhu-Jun Yao, Richard P. Hsung
Edizione [First edition.]
Pubbl/distr/stampa Hoboken, NJ : , : Wiley, , 2018
Descrizione fisica 1 online resource (514 pages)
Disciplina 547/.2
Soggetto topico Natural products - Synthesis
Organic compounds - Synthesis
ISBN 1-118-94021-0
1-118-94020-2
1-118-94022-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910824473303321
Hoboken, NJ : , : Wiley, , 2018
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Pubbl/distr/stampa Weinheim, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (659 p.)
Disciplina 547.59
547/.59
Altri autori (Persone) MajumdarKrishna C
ChattopadhyayShital K
Soggetto topico Heterocyclic compounds
Natural products - Synthesis
ISBN 3-527-63489-4
1-283-37054-9
9786613370549
3-527-63490-8
3-527-63488-6
Classificazione VK 5500
VK 7200
VK 8500
540
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems.
Record Nr. UNINA-9910137853203321
Weinheim, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Pubbl/distr/stampa Weinheim, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (659 p.)
Disciplina 547.59
547/.59
Altri autori (Persone) MajumdarKrishna C
ChattopadhyayShital K
Soggetto topico Heterocyclic compounds
Natural products - Synthesis
ISBN 3-527-63489-4
1-283-37054-9
9786613370549
3-527-63490-8
3-527-63488-6
Classificazione VK 5500
VK 7200
VK 8500
540
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems.
Record Nr. UNINA-9910830690903321
Weinheim, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Heterocycles in natural product synthesis / / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Heterocycles in natural product synthesis / / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Pubbl/distr/stampa Weinheim, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (659 p.)
Disciplina 547.59
547/.59
Altri autori (Persone) MajumdarKrishna C
ChattopadhyayShital K
Soggetto topico Heterocyclic compounds
Natural products - Synthesis
ISBN 9786613370549
9783527634897
3527634894
9781283370547
1283370549
9783527634903
3527634908
9783527634880
3527634886
Classificazione VK 5500
VK 7200
VK 8500
540
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems.
Record Nr. UNINA-9911019846803321
Weinheim, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Metathesis in natural product synthesis [[electronic resource] ] : strategies, substrates and catalysts / / edited by Janine Cossy, Stellios Arseniyadis, and Christophe Meyer ; with a foreword by Robert H. Grubbs
Metathesis in natural product synthesis [[electronic resource] ] : strategies, substrates and catalysts / / edited by Janine Cossy, Stellios Arseniyadis, and Christophe Meyer ; with a foreword by Robert H. Grubbs
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2010
Descrizione fisica 1 online resource (414 p.)
Disciplina 547.2
Altri autori (Persone) CossyJanine
ArseniyadisS (Stellios)
MeyerChristophe
Soggetto topico Natural products - Synthesis
Metathesis (Chemistry)
ISBN 3-527-64208-0
1-283-51405-2
9786613826503
3-527-62963-7
3-527-62962-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts; Contents; Foreword; Preface; List of Catalysts; List of Contributors; Abbreviations; 1 Synthesis of Natural Products Containing Medium-size Carbocycles by Ring-closing Alkene Metathesis; 1.1 Introduction; 1.2 Formation of Five-membered Carbocycles by RCM; 1.3 Formation of Six-membered Carbocycles by RCM; 1.4 Formation of Seven-membered Carbocycles by RCM; 1.5 Formation of Eight-membered Carbocycles by RCM; 1.6 Formation of Nine-membered Carbocycles by RCM; 1.7 Formation of 10-membered Carbocycles by RCM
1.8 ConclusionReferences; 2 Natural Products Containing Medium-sized Nitrogen Heterocycles Synthesized by Ring-closing Alkene Metathesis; 2.1 Introduction; 2.2 Five-membered Nitrogen Heterocycles; 2.2.1 Dihydropyrroles; 2.2.2 Pyrrolidine Alkaloids; 2.2.2.1 Pyrrolidines; 2.2.2.2 Dipyrrolidines; 2.2.2.3 Polyhydroxypyrrolidines; 2.2.3 Indolizidine Alkaloids; 2.2.3.1 Polycyclic Indolizidines; 2.2.3.2 Polyhydroxyindolizidines; 2.2.4 Pyrrolizidine Alkaloids; 2.3 Six-membered Nitrogen Heterocycles; 2.3.1 Piperidine Alkaloids; 2.3.1.1 Piperidines; 2.3.1.2 Piperidine Carboxylic Acids
2.3.1.3 Piperidones2.3.1.4 Polyhydroxypiperidines; 2.3.2 Indolizidine Alkaloids; 2.3.3 Quinolizidine Alkaloids; 2.4 Seven-membered Nitrogen Heterocycles; 2.5 Eight-membered Nitrogen Heterocycles; 2.6 Conclusion; References; 3 Synthesis of Natural Products Containing Medium-size Oxygen Heterocycles by Ring-closing Alkene Metathesis; 3.1 Introduction; 3.2 General RCM Approaches to Medium Rings; 3.3 Laurencin; 3.4 Eunicellins/Eleutherobin; 3.5 Helianane; 3.6 Octalactin A; 3.7 Microcarpalide and the Herbarums; 3.8 Marine Ladder Toxins; 3.8.1 Ciguatoxin; 3.8.2 Brevetoxin
3.8.3 Gambierol, Gambieric Acid, Olefinic-ester Cyclizations3.9 Conclusion; Acknowledgments; References; 4 Phosphorus and Sulfur Heterocycles via Ring-closing Metathesis: Application in Natural Product Synthesis; 4.1 Introduction; 4.2 Synthesis and Reactivity of Sultones Derived from RCM; 4.3 Total Synthesis of the Originally Proposed Structure of (±)-Mycothiazole; 4.4 Synthesis and Reactivity of Phosphates from RCM; 4.5 Applications of Phosphate Tethers in the Synthesis of Dolabelide C; 4.6 Conclusion; Acknowledgment; References
5 Synthesis of Natural Products Containing Macrocycles by Alkene Ring-closing Metathesis5.1 Introduction; 5.2 Organization of the Chapter; 5.3 Macrocyclic Polyketides; 5.3.1 Resorcinylic Macrolides; 5.3.2 Salicylate Macrolides; 5.3.3 Other Antibiotic Macrolides; 5.3.4 Macrocyclic Musk; 5.3.5 Epothilones; 5.3.6 Amphidinolides; 5.3.7 Other Polyketides; 5.3.8 Natural Cyclophanes; 5.4 Terpenoids; 5.4.1 Diterpenoids; 5.4.2 Macrocyclic Lipids; 5.5 Macrocycles of Amino Acid Origin; 5.5.1 Macrolactams; 5.5.2 Cyclodepsipeptides; 5.5.3 Alkaloids; 5.6 Macrocyclic Glycolipids; 5.7 Conclusions and Outlook
References
Record Nr. UNINA-9910140481003321
Weinheim, : Wiley-VCH, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Metathesis in natural product synthesis [[electronic resource] ] : strategies, substrates and catalysts / / edited by Janine Cossy, Stellios Arseniyadis, and Christophe Meyer ; with a foreword by Robert H. Grubbs
Metathesis in natural product synthesis [[electronic resource] ] : strategies, substrates and catalysts / / edited by Janine Cossy, Stellios Arseniyadis, and Christophe Meyer ; with a foreword by Robert H. Grubbs
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2010
Descrizione fisica 1 online resource (414 p.)
Disciplina 547.2
Altri autori (Persone) CossyJanine
ArseniyadisS (Stellios)
MeyerChristophe
Soggetto topico Natural products - Synthesis
Metathesis (Chemistry)
ISBN 3-527-64208-0
1-283-51405-2
9786613826503
3-527-62963-7
3-527-62962-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts; Contents; Foreword; Preface; List of Catalysts; List of Contributors; Abbreviations; 1 Synthesis of Natural Products Containing Medium-size Carbocycles by Ring-closing Alkene Metathesis; 1.1 Introduction; 1.2 Formation of Five-membered Carbocycles by RCM; 1.3 Formation of Six-membered Carbocycles by RCM; 1.4 Formation of Seven-membered Carbocycles by RCM; 1.5 Formation of Eight-membered Carbocycles by RCM; 1.6 Formation of Nine-membered Carbocycles by RCM; 1.7 Formation of 10-membered Carbocycles by RCM
1.8 ConclusionReferences; 2 Natural Products Containing Medium-sized Nitrogen Heterocycles Synthesized by Ring-closing Alkene Metathesis; 2.1 Introduction; 2.2 Five-membered Nitrogen Heterocycles; 2.2.1 Dihydropyrroles; 2.2.2 Pyrrolidine Alkaloids; 2.2.2.1 Pyrrolidines; 2.2.2.2 Dipyrrolidines; 2.2.2.3 Polyhydroxypyrrolidines; 2.2.3 Indolizidine Alkaloids; 2.2.3.1 Polycyclic Indolizidines; 2.2.3.2 Polyhydroxyindolizidines; 2.2.4 Pyrrolizidine Alkaloids; 2.3 Six-membered Nitrogen Heterocycles; 2.3.1 Piperidine Alkaloids; 2.3.1.1 Piperidines; 2.3.1.2 Piperidine Carboxylic Acids
2.3.1.3 Piperidones2.3.1.4 Polyhydroxypiperidines; 2.3.2 Indolizidine Alkaloids; 2.3.3 Quinolizidine Alkaloids; 2.4 Seven-membered Nitrogen Heterocycles; 2.5 Eight-membered Nitrogen Heterocycles; 2.6 Conclusion; References; 3 Synthesis of Natural Products Containing Medium-size Oxygen Heterocycles by Ring-closing Alkene Metathesis; 3.1 Introduction; 3.2 General RCM Approaches to Medium Rings; 3.3 Laurencin; 3.4 Eunicellins/Eleutherobin; 3.5 Helianane; 3.6 Octalactin A; 3.7 Microcarpalide and the Herbarums; 3.8 Marine Ladder Toxins; 3.8.1 Ciguatoxin; 3.8.2 Brevetoxin
3.8.3 Gambierol, Gambieric Acid, Olefinic-ester Cyclizations3.9 Conclusion; Acknowledgments; References; 4 Phosphorus and Sulfur Heterocycles via Ring-closing Metathesis: Application in Natural Product Synthesis; 4.1 Introduction; 4.2 Synthesis and Reactivity of Sultones Derived from RCM; 4.3 Total Synthesis of the Originally Proposed Structure of (±)-Mycothiazole; 4.4 Synthesis and Reactivity of Phosphates from RCM; 4.5 Applications of Phosphate Tethers in the Synthesis of Dolabelide C; 4.6 Conclusion; Acknowledgment; References
5 Synthesis of Natural Products Containing Macrocycles by Alkene Ring-closing Metathesis5.1 Introduction; 5.2 Organization of the Chapter; 5.3 Macrocyclic Polyketides; 5.3.1 Resorcinylic Macrolides; 5.3.2 Salicylate Macrolides; 5.3.3 Other Antibiotic Macrolides; 5.3.4 Macrocyclic Musk; 5.3.5 Epothilones; 5.3.6 Amphidinolides; 5.3.7 Other Polyketides; 5.3.8 Natural Cyclophanes; 5.4 Terpenoids; 5.4.1 Diterpenoids; 5.4.2 Macrocyclic Lipids; 5.5 Macrocycles of Amino Acid Origin; 5.5.1 Macrolactams; 5.5.2 Cyclodepsipeptides; 5.5.3 Alkaloids; 5.6 Macrocyclic Glycolipids; 5.7 Conclusions and Outlook
References
Record Nr. UNINA-9910830522703321
Weinheim, : Wiley-VCH, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Metathesis in natural product synthesis : strategies, substrates and catalysts / / edited by Janine Cossy, Stellios Arseniyadis, and Christophe Meyer ; with a foreword by Robert H. Grubbs
Metathesis in natural product synthesis : strategies, substrates and catalysts / / edited by Janine Cossy, Stellios Arseniyadis, and Christophe Meyer ; with a foreword by Robert H. Grubbs
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2010
Descrizione fisica 1 online resource (414 p.)
Disciplina 547.2
Altri autori (Persone) CossyJanine
ArseniyadisS (Stellios)
MeyerChristophe
Soggetto topico Natural products - Synthesis
Metathesis (Chemistry)
ISBN 9786613826503
9783527642083
3527642080
9781283514057
1283514052
9783527629633
3527629637
9783527629626
3527629629
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts; Contents; Foreword; Preface; List of Catalysts; List of Contributors; Abbreviations; 1 Synthesis of Natural Products Containing Medium-size Carbocycles by Ring-closing Alkene Metathesis; 1.1 Introduction; 1.2 Formation of Five-membered Carbocycles by RCM; 1.3 Formation of Six-membered Carbocycles by RCM; 1.4 Formation of Seven-membered Carbocycles by RCM; 1.5 Formation of Eight-membered Carbocycles by RCM; 1.6 Formation of Nine-membered Carbocycles by RCM; 1.7 Formation of 10-membered Carbocycles by RCM
1.8 ConclusionReferences; 2 Natural Products Containing Medium-sized Nitrogen Heterocycles Synthesized by Ring-closing Alkene Metathesis; 2.1 Introduction; 2.2 Five-membered Nitrogen Heterocycles; 2.2.1 Dihydropyrroles; 2.2.2 Pyrrolidine Alkaloids; 2.2.2.1 Pyrrolidines; 2.2.2.2 Dipyrrolidines; 2.2.2.3 Polyhydroxypyrrolidines; 2.2.3 Indolizidine Alkaloids; 2.2.3.1 Polycyclic Indolizidines; 2.2.3.2 Polyhydroxyindolizidines; 2.2.4 Pyrrolizidine Alkaloids; 2.3 Six-membered Nitrogen Heterocycles; 2.3.1 Piperidine Alkaloids; 2.3.1.1 Piperidines; 2.3.1.2 Piperidine Carboxylic Acids
2.3.1.3 Piperidones2.3.1.4 Polyhydroxypiperidines; 2.3.2 Indolizidine Alkaloids; 2.3.3 Quinolizidine Alkaloids; 2.4 Seven-membered Nitrogen Heterocycles; 2.5 Eight-membered Nitrogen Heterocycles; 2.6 Conclusion; References; 3 Synthesis of Natural Products Containing Medium-size Oxygen Heterocycles by Ring-closing Alkene Metathesis; 3.1 Introduction; 3.2 General RCM Approaches to Medium Rings; 3.3 Laurencin; 3.4 Eunicellins/Eleutherobin; 3.5 Helianane; 3.6 Octalactin A; 3.7 Microcarpalide and the Herbarums; 3.8 Marine Ladder Toxins; 3.8.1 Ciguatoxin; 3.8.2 Brevetoxin
3.8.3 Gambierol, Gambieric Acid, Olefinic-ester Cyclizations3.9 Conclusion; Acknowledgments; References; 4 Phosphorus and Sulfur Heterocycles via Ring-closing Metathesis: Application in Natural Product Synthesis; 4.1 Introduction; 4.2 Synthesis and Reactivity of Sultones Derived from RCM; 4.3 Total Synthesis of the Originally Proposed Structure of (±)-Mycothiazole; 4.4 Synthesis and Reactivity of Phosphates from RCM; 4.5 Applications of Phosphate Tethers in the Synthesis of Dolabelide C; 4.6 Conclusion; Acknowledgment; References
5 Synthesis of Natural Products Containing Macrocycles by Alkene Ring-closing Metathesis5.1 Introduction; 5.2 Organization of the Chapter; 5.3 Macrocyclic Polyketides; 5.3.1 Resorcinylic Macrolides; 5.3.2 Salicylate Macrolides; 5.3.3 Other Antibiotic Macrolides; 5.3.4 Macrocyclic Musk; 5.3.5 Epothilones; 5.3.6 Amphidinolides; 5.3.7 Other Polyketides; 5.3.8 Natural Cyclophanes; 5.4 Terpenoids; 5.4.1 Diterpenoids; 5.4.2 Macrocyclic Lipids; 5.5 Macrocycles of Amino Acid Origin; 5.5.1 Macrolactams; 5.5.2 Cyclodepsipeptides; 5.5.3 Alkaloids; 5.6 Macrocyclic Glycolipids; 5.7 Conclusions and Outlook
References
Record Nr. UNINA-9911019729603321
Weinheim, : Wiley-VCH, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Natural products : the secondary metabolites / James R. Hanson
Natural products : the secondary metabolites / James R. Hanson
Autore Hanson, James R.
Pubbl/distr/stampa Cambridge : Royal Society of chemistry, 2003
Descrizione fisica vi, 147 p. : ill. ; 25 cm
Disciplina 547.7
Collana Tutorial chemistry texts ; 17
Soggetto topico Metabolites
Natural products - Analysis
Natural products - Synthesis
ISBN 0854044906
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISALENTO-991001324959707536
Hanson, James R.  
Cambridge : Royal Society of chemistry, 2003
Materiale a stampa
Lo trovi qui: Univ. del Salento
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