Copper-Catalyzed Multi-Component Reactions : Synthesis of Nitrogen-Containing Polycyclic Compounds
A copper-catalyzed direct synthesis of 2-(aminomethyl)indoles by catalytic domino reaction including multi-component coupling was developed, and is the first example of a three-component indole formation without producing salts as a byproduct. Based on this reaction, a copper-catalyzed synthesis of...
Enregistré dans:
| Hovedforfatter: | |
|---|---|
| Format: | Livre numérique |
| Sprog: | Anglais |
| Udgivet: |
Berlin, Heidelberg :
Springer Berlin Heidelberg
[20..].
Cham : Springer Nature |
| Udgivelse: | 1st ed. 2011. |
| Serier: | Springer Theses, Recognizing Outstanding Ph.D. Research
|
| Online adgang: | Accès sur la plateforme de l'éditeur Accès sur la plateforme Istex Accès Université d'Orléans Accès INSA CVL |
| Kommentar: |
Archives Springer e-books (Licence nationale) Archives Springer e-books (Licence nationale) |
| Autres localisations: | Voir dans le Sudoc |
| Edition sous un autre format: | • Copper-Catalyzed Multi-Component Reactions, Texte imprimé, 9783642154720 • Copper-Catalyzed Multi-Component Reactions, Texte imprimé, 9783642267017 • Copper-Catalyzed Multi-Component Reactions, Texte imprimé, 9783642154744 |
| LEADER | 03112nam a22003377a 4500 | ||
|---|---|---|---|
| 001 | 968198 | ||
| 008 | 110208q2000 xx ||| |||| 00| 0 eng d | ||
| 009 | PPN149906188 | ||
| 020 | |a 9783642154737 | ||
| 041 | 0 | |a eng | |
| 082 | |a 547 | ||
| 100 | 1 | |a Ohta, Yusuke. | |
| 245 | 1 | 0 | |a Copper-Catalyzed Multi-Component Reactions : |b Synthesis of Nitrogen-Containing Polycyclic Compounds |c by Yusuke Ohta. |
| 250 | |a 1st ed. 2011. | ||
| 260 | |a Berlin, Heidelberg : |b Springer Berlin Heidelberg. | ||
| 260 | |a Cham : |b Springer Nature, |c [20..]. | ||
| 490 | 0 | |a Springer Theses, Recognizing Outstanding Ph.D. Research |x 2190-5061 | |
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 506 | |a Accès en ligne pour les établissements français bénéficiaires des licences nationales | ||
| 506 | |a Accès soumis à abonnement pour tout autre établissement | ||
| 506 | |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales. https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 | ||
| 520 | |a A copper-catalyzed direct synthesis of 2-(aminomethyl)indoles by catalytic domino reaction including multi-component coupling was developed, and is the first example of a three-component indole formation without producing salts as a byproduct. Based on this reaction, a copper-catalyzed synthesis of 3-(aminomethyl)isoquinoline was accomplished which represents an unprecedented isoquinoline synthesis through a four-component coupling reaction. Following these results, extensive application studies using one-pot palladium-, acid-, or base-promoted cyclization revealed that indole- or isoquinoline-fused polycyclic compounds can be readily synthesized through multi-component reactions. As the concept of Green Chemistry becomes ever more important, these findings may provide efficient and atom-economical approaches to the diversity-oriented synthesis of bioactive compounds containing a complex structure. This could lead to development of promising drug leads with structural complexity. The work of this thesis will go on to inspire the synthetic research of many readers. | ||
| 776 | 0 | |t Copper-Catalyzed Multi-Component Reactions |b Texte imprimé |z 9783642154720 | |
| 776 | 0 | |t Copper-Catalyzed Multi-Component Reactions |b Texte imprimé |z 9783642267017 | |
| 776 | 0 | |t Copper-Catalyzed Multi-Component Reactions |b Texte imprimé |z 9783642154744 | |
| 856 | 4 | |q PDF |u https://doi.org/10.1007/978-3-642-15473-7 |z Accès sur la plateforme de l'éditeur | |
| 856 | 4 | |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-P4BJSTFW-D |z Accès sur la plateforme Istex | |
| 856 | 4 | |5 452349901:750623292 |u https://ezproxy.univ-orleans.fr/login?url=https://dx.doi.org/10.1007/978-3-642-15473-7 |z Accès Université d'Orléans | |
| 856 | 4 | |5 180339901:753980886 |u https://ezproxy.insa-cvl.fr/login?qurl=https://dx.doi.org/10.1007/978-3-642-15473-7 |z Accès INSA CVL | |
| 997 | |0 968198 |1 Livre numérique |a Ressource numérique |b INSA |b ENSA |c 0/Bibliothèque numérique/ |c 1/Bibliothèque numérique/Autre ressource numérique/ | ||

