Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Acetylene chemistry [[electronic resource] ] : chemistry, biology, and material science / / edited by F. Diederich, P.J. Stang, R.R. Tykwinski
| Acetylene chemistry [[electronic resource] ] : chemistry, biology, and material science / / edited by F. Diederich, P.J. Stang, R.R. Tykwinski |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2005 |
| Descrizione fisica | 1 online resource (530 p.) |
| Disciplina | 547.413 |
| Altri autori (Persone) |
DiederichFrançois
StangPeter J TykwinskiR. R (Rik R.) |
| Soggetto topico |
Acetylene
Alkynes |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-51994-0
9786610519941 3-527-60548-7 3-527-60470-7 |
| Classificazione | 35.68 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Acetylene Chemistry; Preface; Contents; Symbols and Abbreviations; List of Contributors; 1 Theoretical Studies on Acetylenic Scaffolds; 1.1 Introduction; 1.2 Linear Acetylenic Scaffolds; 1.2.1 The Dicarbon Molecule and Acetylene; 1.2.2 Uncapped Pure sp Carbon Chains; 1.2.3 Capped All-sp Oligoacetylenic Chains; 1.2.4 Hybrid sp-sp(2) Oligoacetylenic Molecules; 1.2.5 Hybrid sp-sp(3) Oligoacetylenic Molecules; 1.3 Cyclic Acetylenic Scaffolds; 1.3.1 Hybrid sp-sp(3) Rings; 1.3.2 Hybrid sp-sp(2) Rings (Dehydroannulenes); 1.3.3 carbo-Heteroannulenes; 1.4 Star-Shaped Acetylenic Scaffolds
1.4.1 Atomic Cores1.4.2 Rod Cores; 1.4.3 Cyclic Cores; 1.5 Cage Acetylenic Scaffolds; 1.6 Conclusion; Acknowledgements; 2 Synthesis of Heterocycles and Carbocycles by Electrophilic Cyclization of Alkynes; 2.1 Introduction; 2.2 Cyclization of Oxygen Compounds; 2.2.1 Cyclization of Acetylenic Alcohols; 2.2.2 Cyclization of Acetylenic Phenols; 2.2.3 Cyclization of Acetylenic Ethers; 2.2.4 Cyclization of Acetylenic Acids and Derivatives; 2.2.5 Cyclization of Acetylenic Aldehydes and Ketones; 2.3 Cyclization of Sulfur and Selenium Compounds; 2.4 Cyclization of Nitrogen Compounds 2.4.1 Cyclization of Acetylenic Amines2.4.2 Cyclization of Acetylenic Amides; 2.4.3 Cyclization of Acetylenic Carbamates; 2.4.4 Cyclization of Acetylenic Sulfonamides; 2.4.5 Cyclization of Acetylenic Enamines and Imines; 2.4.6 Cyclization of Other Acetylenic Nitrogen Functional Groups; 2.5 Cyclization of Carbon onto Acetylenes; 2.5.1 Cyclization of Acetylenic Carbonyl Compounds and Derivatives; 2.5.2 Cyclization of Diacetylenes; 2.5.3 Cyclization of Aryl Acetylenes; 2.5.4 Cyclization of Acetylenic Organometallics; 2.6 Conclusions; 2.7 Representative Experimental Procedures 2.7.1 Synthesis of α-Methylene-γ-butyrolactones by Carbonylation of 1-Alkyn-4-ols2.7.2 Synthesis of 1-Alkoxyisochromenes by Cyclization of 2-(1-Alkynyl)benzaldehydes; 2.7.3 Synthesis of 3-Aryl(vinylic)indoles by Palladium-catalyzed Cross-coupling of Aryl Halides or Vinylic Triflates and 2-(1-Alkynyl)trifluoroacetanilides; 2.7.4 Synthesis of Pyridines by the Gold-catalyzed Cross-coupling of Ketones and Propargyl Amine; 2.7.5 Synthesis of 4-Iodoisoquinolines by the Cyclization of Iminoalkynes; 2.7.6 Synthesis of Cyclic Amines by Acetylene-Iminium Ion Cyclizations; Acknowledgements 3 Addition of Terminal Acetylides to CO and CN Electrophiles3.1 Introduction; 3.2 Background; 3.3 Additions with Stoichiometric Amounts of Metal Acetylides; 3.4 Nucleophilic CO Additions involving the Use of Zn(II) Salts; 3.5 Acetylene Additions to CN Electrophiles; 3.6 Conclusion; 3.7 Experimental Procedures; 3.7.1 General Procedure for the Enantioselective Alkynylation of Aldehydes by the Use of Stoichiometric Amounts of Zn(OTf)(2); 3.7.2 General Procedure for the Zn(OTf)(2)-Catalyzed Enantioselective Alkynylation of Aldehydes 3.7.3 General Procedure for the Enantioselective Alkynylation of Ketones Catalyzed by Zn(salen) Complexes |
| Record Nr. | UNINA-9910144327303321 |
| Weinheim, : Wiley-VCH, c2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Acetylene chemistry [[electronic resource] ] : chemistry, biology, and material science / / edited by F. Diederich, P.J. Stang, R.R. Tykwinski
| Acetylene chemistry [[electronic resource] ] : chemistry, biology, and material science / / edited by F. Diederich, P.J. Stang, R.R. Tykwinski |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2005 |
| Descrizione fisica | 1 online resource (530 p.) |
| Disciplina | 547.413 |
| Altri autori (Persone) |
DiederichFrançois
StangPeter J TykwinskiR. R (Rik R.) |
| Soggetto topico |
Acetylene
Alkynes |
| ISBN |
1-280-51994-0
9786610519941 3-527-60548-7 3-527-60470-7 |
| Classificazione | 35.68 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Acetylene Chemistry; Preface; Contents; Symbols and Abbreviations; List of Contributors; 1 Theoretical Studies on Acetylenic Scaffolds; 1.1 Introduction; 1.2 Linear Acetylenic Scaffolds; 1.2.1 The Dicarbon Molecule and Acetylene; 1.2.2 Uncapped Pure sp Carbon Chains; 1.2.3 Capped All-sp Oligoacetylenic Chains; 1.2.4 Hybrid sp-sp(2) Oligoacetylenic Molecules; 1.2.5 Hybrid sp-sp(3) Oligoacetylenic Molecules; 1.3 Cyclic Acetylenic Scaffolds; 1.3.1 Hybrid sp-sp(3) Rings; 1.3.2 Hybrid sp-sp(2) Rings (Dehydroannulenes); 1.3.3 carbo-Heteroannulenes; 1.4 Star-Shaped Acetylenic Scaffolds
1.4.1 Atomic Cores1.4.2 Rod Cores; 1.4.3 Cyclic Cores; 1.5 Cage Acetylenic Scaffolds; 1.6 Conclusion; Acknowledgements; 2 Synthesis of Heterocycles and Carbocycles by Electrophilic Cyclization of Alkynes; 2.1 Introduction; 2.2 Cyclization of Oxygen Compounds; 2.2.1 Cyclization of Acetylenic Alcohols; 2.2.2 Cyclization of Acetylenic Phenols; 2.2.3 Cyclization of Acetylenic Ethers; 2.2.4 Cyclization of Acetylenic Acids and Derivatives; 2.2.5 Cyclization of Acetylenic Aldehydes and Ketones; 2.3 Cyclization of Sulfur and Selenium Compounds; 2.4 Cyclization of Nitrogen Compounds 2.4.1 Cyclization of Acetylenic Amines2.4.2 Cyclization of Acetylenic Amides; 2.4.3 Cyclization of Acetylenic Carbamates; 2.4.4 Cyclization of Acetylenic Sulfonamides; 2.4.5 Cyclization of Acetylenic Enamines and Imines; 2.4.6 Cyclization of Other Acetylenic Nitrogen Functional Groups; 2.5 Cyclization of Carbon onto Acetylenes; 2.5.1 Cyclization of Acetylenic Carbonyl Compounds and Derivatives; 2.5.2 Cyclization of Diacetylenes; 2.5.3 Cyclization of Aryl Acetylenes; 2.5.4 Cyclization of Acetylenic Organometallics; 2.6 Conclusions; 2.7 Representative Experimental Procedures 2.7.1 Synthesis of α-Methylene-γ-butyrolactones by Carbonylation of 1-Alkyn-4-ols2.7.2 Synthesis of 1-Alkoxyisochromenes by Cyclization of 2-(1-Alkynyl)benzaldehydes; 2.7.3 Synthesis of 3-Aryl(vinylic)indoles by Palladium-catalyzed Cross-coupling of Aryl Halides or Vinylic Triflates and 2-(1-Alkynyl)trifluoroacetanilides; 2.7.4 Synthesis of Pyridines by the Gold-catalyzed Cross-coupling of Ketones and Propargyl Amine; 2.7.5 Synthesis of 4-Iodoisoquinolines by the Cyclization of Iminoalkynes; 2.7.6 Synthesis of Cyclic Amines by Acetylene-Iminium Ion Cyclizations; Acknowledgements 3 Addition of Terminal Acetylides to CO and CN Electrophiles3.1 Introduction; 3.2 Background; 3.3 Additions with Stoichiometric Amounts of Metal Acetylides; 3.4 Nucleophilic CO Additions involving the Use of Zn(II) Salts; 3.5 Acetylene Additions to CN Electrophiles; 3.6 Conclusion; 3.7 Experimental Procedures; 3.7.1 General Procedure for the Enantioselective Alkynylation of Aldehydes by the Use of Stoichiometric Amounts of Zn(OTf)(2); 3.7.2 General Procedure for the Zn(OTf)(2)-Catalyzed Enantioselective Alkynylation of Aldehydes 3.7.3 General Procedure for the Enantioselective Alkynylation of Ketones Catalyzed by Zn(salen) Complexes |
| Record Nr. | UNINA-9910829862803321 |
| Weinheim, : Wiley-VCH, c2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Acetylene chemistry : chemistry, biology, and material science / / edited by F. Diederich, P.J. Stang, R.R. Tykwinski
| Acetylene chemistry : chemistry, biology, and material science / / edited by F. Diederich, P.J. Stang, R.R. Tykwinski |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2005 |
| Descrizione fisica | 1 online resource (530 p.) |
| Disciplina | 547.413 |
| Altri autori (Persone) |
DiederichFrancois
StangPeter J TykwinskiR. R (Rik R.) |
| Soggetto topico |
Acetylene
Alkynes |
| ISBN |
1-280-51994-0
9786610519941 3-527-60548-7 3-527-60470-7 |
| Classificazione | 35.68 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Acetylene Chemistry; Preface; Contents; Symbols and Abbreviations; List of Contributors; 1 Theoretical Studies on Acetylenic Scaffolds; 1.1 Introduction; 1.2 Linear Acetylenic Scaffolds; 1.2.1 The Dicarbon Molecule and Acetylene; 1.2.2 Uncapped Pure sp Carbon Chains; 1.2.3 Capped All-sp Oligoacetylenic Chains; 1.2.4 Hybrid sp-sp(2) Oligoacetylenic Molecules; 1.2.5 Hybrid sp-sp(3) Oligoacetylenic Molecules; 1.3 Cyclic Acetylenic Scaffolds; 1.3.1 Hybrid sp-sp(3) Rings; 1.3.2 Hybrid sp-sp(2) Rings (Dehydroannulenes); 1.3.3 carbo-Heteroannulenes; 1.4 Star-Shaped Acetylenic Scaffolds
1.4.1 Atomic Cores1.4.2 Rod Cores; 1.4.3 Cyclic Cores; 1.5 Cage Acetylenic Scaffolds; 1.6 Conclusion; Acknowledgements; 2 Synthesis of Heterocycles and Carbocycles by Electrophilic Cyclization of Alkynes; 2.1 Introduction; 2.2 Cyclization of Oxygen Compounds; 2.2.1 Cyclization of Acetylenic Alcohols; 2.2.2 Cyclization of Acetylenic Phenols; 2.2.3 Cyclization of Acetylenic Ethers; 2.2.4 Cyclization of Acetylenic Acids and Derivatives; 2.2.5 Cyclization of Acetylenic Aldehydes and Ketones; 2.3 Cyclization of Sulfur and Selenium Compounds; 2.4 Cyclization of Nitrogen Compounds 2.4.1 Cyclization of Acetylenic Amines2.4.2 Cyclization of Acetylenic Amides; 2.4.3 Cyclization of Acetylenic Carbamates; 2.4.4 Cyclization of Acetylenic Sulfonamides; 2.4.5 Cyclization of Acetylenic Enamines and Imines; 2.4.6 Cyclization of Other Acetylenic Nitrogen Functional Groups; 2.5 Cyclization of Carbon onto Acetylenes; 2.5.1 Cyclization of Acetylenic Carbonyl Compounds and Derivatives; 2.5.2 Cyclization of Diacetylenes; 2.5.3 Cyclization of Aryl Acetylenes; 2.5.4 Cyclization of Acetylenic Organometallics; 2.6 Conclusions; 2.7 Representative Experimental Procedures 2.7.1 Synthesis of α-Methylene-γ-butyrolactones by Carbonylation of 1-Alkyn-4-ols2.7.2 Synthesis of 1-Alkoxyisochromenes by Cyclization of 2-(1-Alkynyl)benzaldehydes; 2.7.3 Synthesis of 3-Aryl(vinylic)indoles by Palladium-catalyzed Cross-coupling of Aryl Halides or Vinylic Triflates and 2-(1-Alkynyl)trifluoroacetanilides; 2.7.4 Synthesis of Pyridines by the Gold-catalyzed Cross-coupling of Ketones and Propargyl Amine; 2.7.5 Synthesis of 4-Iodoisoquinolines by the Cyclization of Iminoalkynes; 2.7.6 Synthesis of Cyclic Amines by Acetylene-Iminium Ion Cyclizations; Acknowledgements 3 Addition of Terminal Acetylides to CO and CN Electrophiles3.1 Introduction; 3.2 Background; 3.3 Additions with Stoichiometric Amounts of Metal Acetylides; 3.4 Nucleophilic CO Additions involving the Use of Zn(II) Salts; 3.5 Acetylene Additions to CN Electrophiles; 3.6 Conclusion; 3.7 Experimental Procedures; 3.7.1 General Procedure for the Enantioselective Alkynylation of Aldehydes by the Use of Stoichiometric Amounts of Zn(OTf)(2); 3.7.2 General Procedure for the Zn(OTf)(2)-Catalyzed Enantioselective Alkynylation of Aldehydes 3.7.3 General Procedure for the Enantioselective Alkynylation of Ketones Catalyzed by Zn(salen) Complexes |
| Record Nr. | UNINA-9910876680203321 |
| Weinheim, : Wiley-VCH, c2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby
| Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby |
| Autore | Maretina Irina A |
| Pubbl/distr/stampa | Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014 |
| Descrizione fisica | 1 online resource (312 p.) |
| Disciplina | 547/.413 |
| Altri autori (Persone) |
TebbyJohn C. <1933->
IoninB. I |
| Soggetto topico |
Alkynes
Ring formation (Chemistry) |
| ISBN |
1-118-70929-2
1-118-70931-4 1-118-70933-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Alkynes in Cycloadditions; Contents; Preface; Acknowledgments; Biography; 1 Introduction; 2 Regioselective Syntheses of Polysubstituted Benzenes Catalyzed by Transition Metal Complexes; 2.1 [2+2+2] Cycloaddition Reactions of Acetylenes; 2.1.1 Reactions of Alkynes with Metallocyclopentadiene as an Intermediate; 2.1.2 Intra-intermolecular [2+2+2] Cycloaddition of Alkynes; 2.2 Stereochemical Aspect of Intramolecular and Intermolecular Reactions of Diynes with Monoalkynes; 2.2.1 Strategy of Enantioselective [2+2+2] Cycloaddition; 2.3 Heteroatom Bound to the Triple Bond
2.3.1 Nitrogen-Containing Substrates2.3.2 [2+2+2] Cycloadditions of Alkynes to Nitriles: Synthesis of Pyridines; 2.4 Heterohelicens. Asymmetric Syntheses; 2.4.1 Oxygen-Containing Helicens; 2.4.2 Nitrogen-Containing Helicens. Helical Dications; 2.5 Aromatic Rings with Boron and Silicon Substituents; 2.6 [2+2+2] Cycloaddition Reactions of 1-Alkynylphosphines and Their Derivatives; 2.7 Intramolecular [2+2+2] Cycloaddition of Diynes to Alkenes; 2.7.1 Allene as an Alkene Component; 2.7.2 Formation of Polycyclic Cyclohexadienes by Ru-catalyzed Cascade Reactions of 1,6-Diynes and Alkenes 2.7.3 Stereochemical Aspects of the Reaction of Diynes with Alkenes2.7.4 Hetero-[2+2+2] Cycloaddition of Alkynes to Compounds with a Multiple Carbon-Heteroatom Bond; 2.8 Reactions of [4+2] Cycloaddition and Other Approaches to the Synthesis of Polysubstituted Benzenes; 2.8.1 Reactions of Conjugated Enynes; 2.8.2 Acceleration of Pd-catalyzed [4+2]-Benzannulation in the Reaction of Enynes and Diynes in the Presence of Lewis Acids and Bronsted Bases; 2.9 Combined Reactions 2.9.1 Formal [4+2+2] Cycloaddition of 1,6-Diynes to 1,3-Dienes Catalyzed by Ru: Formation of Cyclooctatrienes and Vinylcyclohexadienes2.9.2 Formation of Eight-Membered Ring Systems by [4+2+2] Annulation; 2.9.3 AuBr3 (AlCl3)- and Cu(OTf)2-Catalyzed [4+2] Cycloaddition of Alkynyl- and Alkenyl-Enynones and Enynals: An Approach to Functionalized Polycyclic Hydrocarbons; 2.10 Construction of Polycyclic Systems; 2.10.1 Strategies for the Synthesis of Steroid Systems by Co-catalyzed [2+2+2] Cycloaddition of Nonconjugated Enyne-Allenes and Enediynes 2.10.2 Cobalt(I)-Mediated [2+2+2] Cyclization of Allene-Diynes: A Diastereoselective Approach to 11-aryl Steroid Core. 11-Aryl-Substituted Steroid Systems by Co-catalyzed [2+2+2] Cyclization of Allene-Diynes2.10.3 Synthesis of (3S)-hydroxyandrosta-5,7-diene-17-ones via Intramolecular Cobalt-Mediated [2+2+2] Cycloaddition; 2.10.4 Intramolecular Cycloaddition of Nonconjugated Enediynes of a Higher Order as a Route to Functionalized Condensed Polycyclic Systems; 2.10.5 A Strategy for the Synthesis of Aromatic Molecular-Bowl Hydrocarbons 2.10.6 A Route to Archimedenes: Total Synthesis of C3h-symmetric [7]phenylenes |
| Record Nr. | UNINA-9910138996803321 |
Maretina Irina A
|
||
| Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby
| Alkynes in cycloadditions / / author, Irina A. Maretina ; translated from the Russian by Boris I. Ionin ; consulting editor, John C. Tebby |
| Autore | Maretina Irina A |
| Pubbl/distr/stampa | Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014 |
| Descrizione fisica | 1 online resource (312 p.) |
| Disciplina | 547/.413 |
| Altri autori (Persone) |
TebbyJohn C. <1933->
IoninB. I |
| Soggetto topico |
Alkynes
Ring formation (Chemistry) |
| ISBN |
1-118-70929-2
1-118-70931-4 1-118-70933-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Alkynes in Cycloadditions; Contents; Preface; Acknowledgments; Biography; 1 Introduction; 2 Regioselective Syntheses of Polysubstituted Benzenes Catalyzed by Transition Metal Complexes; 2.1 [2+2+2] Cycloaddition Reactions of Acetylenes; 2.1.1 Reactions of Alkynes with Metallocyclopentadiene as an Intermediate; 2.1.2 Intra-intermolecular [2+2+2] Cycloaddition of Alkynes; 2.2 Stereochemical Aspect of Intramolecular and Intermolecular Reactions of Diynes with Monoalkynes; 2.2.1 Strategy of Enantioselective [2+2+2] Cycloaddition; 2.3 Heteroatom Bound to the Triple Bond
2.3.1 Nitrogen-Containing Substrates2.3.2 [2+2+2] Cycloadditions of Alkynes to Nitriles: Synthesis of Pyridines; 2.4 Heterohelicens. Asymmetric Syntheses; 2.4.1 Oxygen-Containing Helicens; 2.4.2 Nitrogen-Containing Helicens. Helical Dications; 2.5 Aromatic Rings with Boron and Silicon Substituents; 2.6 [2+2+2] Cycloaddition Reactions of 1-Alkynylphosphines and Their Derivatives; 2.7 Intramolecular [2+2+2] Cycloaddition of Diynes to Alkenes; 2.7.1 Allene as an Alkene Component; 2.7.2 Formation of Polycyclic Cyclohexadienes by Ru-catalyzed Cascade Reactions of 1,6-Diynes and Alkenes 2.7.3 Stereochemical Aspects of the Reaction of Diynes with Alkenes2.7.4 Hetero-[2+2+2] Cycloaddition of Alkynes to Compounds with a Multiple Carbon-Heteroatom Bond; 2.8 Reactions of [4+2] Cycloaddition and Other Approaches to the Synthesis of Polysubstituted Benzenes; 2.8.1 Reactions of Conjugated Enynes; 2.8.2 Acceleration of Pd-catalyzed [4+2]-Benzannulation in the Reaction of Enynes and Diynes in the Presence of Lewis Acids and Bronsted Bases; 2.9 Combined Reactions 2.9.1 Formal [4+2+2] Cycloaddition of 1,6-Diynes to 1,3-Dienes Catalyzed by Ru: Formation of Cyclooctatrienes and Vinylcyclohexadienes2.9.2 Formation of Eight-Membered Ring Systems by [4+2+2] Annulation; 2.9.3 AuBr3 (AlCl3)- and Cu(OTf)2-Catalyzed [4+2] Cycloaddition of Alkynyl- and Alkenyl-Enynones and Enynals: An Approach to Functionalized Polycyclic Hydrocarbons; 2.10 Construction of Polycyclic Systems; 2.10.1 Strategies for the Synthesis of Steroid Systems by Co-catalyzed [2+2+2] Cycloaddition of Nonconjugated Enyne-Allenes and Enediynes 2.10.2 Cobalt(I)-Mediated [2+2+2] Cyclization of Allene-Diynes: A Diastereoselective Approach to 11-aryl Steroid Core. 11-Aryl-Substituted Steroid Systems by Co-catalyzed [2+2+2] Cyclization of Allene-Diynes2.10.3 Synthesis of (3S)-hydroxyandrosta-5,7-diene-17-ones via Intramolecular Cobalt-Mediated [2+2+2] Cycloaddition; 2.10.4 Intramolecular Cycloaddition of Nonconjugated Enediynes of a Higher Order as a Route to Functionalized Condensed Polycyclic Systems; 2.10.5 A Strategy for the Synthesis of Aromatic Molecular-Bowl Hydrocarbons 2.10.6 A Route to Archimedenes: Total Synthesis of C3h-symmetric [7]phenylenes |
| Record Nr. | UNINA-9910826821803321 |
|
Maretina Irina A
|
||
| Chichester, West Sussex : , : John Wiley & Sons, Inc., , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
New gold-catalyzed reactions and applications for the synthesis of alkaloids / / Ana Escribano Cuesta
| New gold-catalyzed reactions and applications for the synthesis of alkaloids / / Ana Escribano Cuesta |
| Autore | Cuesta Ana Escribano |
| Edizione | [1st ed. 2013.] |
| Pubbl/distr/stampa | Cham ; ; New York, : Springer, c2013 |
| Descrizione fisica | 1 online resource (202 p.) |
| Disciplina | 547 |
| Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
| Soggetto topico |
Catalysis
Alkynes |
| ISBN | 3-319-00702-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction -- General Objectives -- Gold(I)-Catalyzed Reactions of 1,6-Enynes with Aldehydes: Cycloaddition versus Metathesis-Type Reactions -- Formation of Cyclobutene Compounds via Gold(I)-Catalyzed Cycloisomerization of 1,n-Enynes -- Approach Toward the Total Synthesis of Lundurines. |
| Record Nr. | UNINA-9910437818103321 |
|
Cuesta Ana Escribano
|
||
| Cham ; ; New York, : Springer, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Soggetto topico
-
Alkynes
(6)
- Acetylene (3)
- Ring formation (Chemistry) (2)
- Catalysis (1)