Click Chemistry ‘CC’ are Cu(I) catalyzed 1,3-dipolar [3+2] cycloaddition between azides and alkynes [CuAAC]. The versatility of CuAAC or ‘click reaction’ seem endless with the discovery and invention of new chemical transformations which meet ‘click’ status, the future looks bright for CC. Recently, Click chemistry has received considerable attention as powerful modular synthesis approach, which has found numerous applications in many areas of modern organic chemistry, drug discovery, radiopharmaceutical sciences and material science. The great success of CC encouraged researchers to develop alternative “spring-loaded” chemical reactions for use in different fields of chemistry. Initially, CuAAC was the only click reaction. In recent years, metal-free [3+2] cycloaddition reactions, Diels–Alder reactions, and thiol-alkene radical addition reactions have come to the fore as click reactions because of their simple synthetic procedures and high yields. Also, these metal-free reactions have wide applicability and are physiologically compatible. Alternative CC expand the opportunities for synthesizing small organic compounds well as tailor-made macromolecules and bioconjugates.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
Click Chemistry ‘CC’ are Cu(I) catalyzed 1,3-dipolar [3+2] cycloaddition between azides and alkynes [CuAAC]. The versatility of CuAAC or ‘click reaction’ seem endless with the discovery and invention of new chemical transformations which meet ‘click’ status, the future looks bright for CC. Recently, Click chemistry has received considerable attention as powerful modular synthesis approach, which has found numerous applications in many areas of modern organic chemistry, drug discovery, radiopharmaceutical sciences and material science. The great success of CC encouraged researchers to develop alternative “spring-loaded” chemical reactions for use in different fields of chemistry. Initially, CuAAC was the only click reaction. In recent years, metal-free [3+2] cycloaddition reactions, Diels–Alder reactions, and thiol-alkene radical addition reactions have come to the fore as click reactions because of their simple synthetic procedures and high yields. Also, these metal-free reactions have wide applicability and are physiologically compatible. Alternative CC expand the opportunities for synthesizing small organic compounds well as tailor-made macromolecules and bioconjugates.
Adel S. El-Azab and Alaa A.-M. Abdel-Aziz, awarded Ph.D. in organic Chemistry in 2001 from Tohoku and Kumamoto Universities, Japan. They are working as Professor at the College of Pharmacy, Al-Azhar and Mansoura Universities, Egypt. Currently, work as staff members at College of Pharmacy, King Saud University, Saudi Arabia
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: El-Azab Adel S.Adel S. El-Azab and Alaa A.-M. Abdel-Aziz, awarded Ph.D. in organic Chemistry in 2001 from Tohoku and Kumamoto Universities, Japan. They are working as Professor at the College of Pharmacy, Al-Azhar and Mansoura Univer. N° de réf. du vendeur 5164558
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Click Chemistry CC are Cu(I) catalyzed 1,3-dipolar [3+2] cycloaddition between azides and alkynes [CuAAC]. The versatility of CuAAC or click reaction seem endless with the discovery and invention of new chemical transformations which meet click status, the future looks bright for CC. Recently, Click chemistry has received considerable attention as powerful modular synthesis approach, which has found numerous applications in many areas of modern organic chemistry, drug discovery, radiopharmaceutical sciences and material science. The great success of CC encouraged researchers to develop alternative spring-loaded chemical reactions for use in different fields of chemistry. Initially, CuAAC was the only click reaction. In recent years, metal-free [3+2] cycloaddition reactions, Diels Alder reactions, and thiol-alkene radical addition reactions have come to the fore as click reactions because of their simple synthetic procedures and high yields. Also, these metal-free reactions have wide applicability and are physiologically compatible. Alternative CC expand the opportunities for synthesizing small organic compounds well as tailor-made macromolecules and bioconjugates. N° de réf. du vendeur 9783659555466
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Taschenbuch. Etat : Neu. Click Chemistry and Applications | Alkynes and Azides Cu(I) Catalyzed Cycloaddition Reaction | Adel S. El-Azab (u. a.) | Taschenbuch | 152 S. | Englisch | 2014 | LAP Lambert Academic Publishing | EAN 9783659555466 | Verantwortliche Person für die EU: LAP Lambert Academic Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. N° de réf. du vendeur 105217334
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