Jason Woolford's thesis describes for the first time, a double [3+2] photocycloaddition of alkenes onto aromatic rings. Modern synthetic chemistry relies on the ability of researchers to uncover new and more efficient ways of creating highly complex structures. This work describes a novel, environmentally friendly photochemical step that converts in one pot, trivial starting materials into otherwise difficult to construct fenstrane frameworks. The rigid cores of these frameworks have significant potential in drug design. Moreover, the novelty of this work overtakes many other methods for the…mehr
Jason Woolford's thesis describes for the first time, a double [3+2] photocycloaddition of alkenes onto aromatic rings. Modern synthetic chemistry relies on the ability of researchers to uncover new and more efficient ways of creating highly complex structures. This work describes a novel, environmentally friendly photochemical step that converts in one pot, trivial starting materials into otherwise difficult to construct fenstrane frameworks. The rigid cores of these frameworks have significant potential in drug design. Moreover, the novelty of this work overtakes many other methods for the creation of chiral centres. No less than seven chiral centres are created in the photochemical step together with the formation of four carbon-carbon bonds and multifused rings. Jason's innovative work has been the subject of several publications in peer-reviewed journals.
Artikelnr. des Verlages: 80074792, 978-3-642-22859-9
2011
Seitenzahl: 200
Erscheinungstermin: 31. August 2011
Englisch
Abmessung: 241mm x 160mm x 14mm
Gewicht: 438g
ISBN-13: 9783642228599
ISBN-10: 3642228593
Artikelnr.: 33695130
Autorenporträt
Jason Woolford's thesis describes for the first time, a double [3+2] photocycloaddition of alkenes onto aromatic rings. Modern snythetic chemistry relies on the ability of researchers to uncover new and more efficient ways of creating highly complex structures. This work describes a novel, environmentally friendly photochemical step that converts in one pot, trivial starting materials into otherwise difficult to construct fenstrane frameworks. The rigid cores of these frameworks have significant potential in drug design. Moreover, the novelty of this work overtakes many other methods for the creation of chiral centres. No less than seven chiral centres are created in the photochemical step together with the formation of four carbon-carbon bonds and multifused rings. Jason's innovative work has been the subject of several publications in peer-reviewed journals.
Inhaltsangabe
Introduction and background.- Discovery of the double [3+2] photocycloaddition.- A brief discussion on fenestranes.- Investigation of the double [3+2] photocycloaddition reaction for the synthesis of fenestranes.- Attempted synthesis of a "criss-cross" double [3+2] photocycloadduct.- Attempts toward the synthesis of alternative structures via the double[3+2] photocycloaddition.- Conclusion.- Experimental.- References.- Appendix I.
Introduction and background.- Discovery of the double [3+2] photocycloaddition.- A brief discussion on fenestranes.- Investigation of the double [3+2] photocycloaddition reaction for the synthesis of fenestranes.- Attempted synthesis of a “criss-cross” double [3+2] photocycloadduct.- Attempts toward the synthesis of alternative structures via the double[3+2] photocycloaddition.- Conclusion.- Experimental.- References.- Appendix I.
Introduction and background.- Discovery of the double [3+2] photocycloaddition.- A brief discussion on fenestranes.- Investigation of the double [3+2] photocycloaddition reaction for the synthesis of fenestranes.- Attempted synthesis of a "criss-cross" double [3+2] photocycloadduct.- Attempts toward the synthesis of alternative structures via the double[3+2] photocycloaddition.- Conclusion.- Experimental.- References.- Appendix I.
Introduction and background.- Discovery of the double [3+2] photocycloaddition.- A brief discussion on fenestranes.- Investigation of the double [3+2] photocycloaddition reaction for the synthesis of fenestranes.- Attempted synthesis of a “criss-cross” double [3+2] photocycloadduct.- Attempts toward the synthesis of alternative structures via the double[3+2] photocycloaddition.- Conclusion.- Experimental.- References.- Appendix I.
Es gelten unsere Allgemeinen Geschäftsbedingungen: www.buecher.de/agb
Impressum
www.buecher.de ist ein Internetauftritt der buecher.de internetstores GmbH
Geschäftsführung: Monica Sawhney | Roland Kölbl | Günter Hilger
Sitz der Gesellschaft: Batheyer Straße 115 - 117, 58099 Hagen
Postanschrift: Bürgermeister-Wegele-Str. 12, 86167 Augsburg
Amtsgericht Hagen HRB 13257
Steuernummer: 321/5800/1497