Organic Syntheses Based on Name Reactions

2. Auflage 2002
ISBN: 978-0-08-043259-5
Verlag: Elsevier Science

Buch, Englisch, 454 Seiten, Format (B × H): 168 mm x 240 mm, Gewicht: 839 g

Since the publication of "Organic Syntheses Based on Name Reactions and Unnamed Reactions"(Volume 11 in the Tetrahedron Organic Chemistry series), there has been a proliferation of discoveries of name reactions in the field of organic chemistry. Hence, this, the second, revised, edition of the text has focused on the ongoing development in this area of research. The revised title reflects the notion whereby many new reagents and reactions are now being referred to by their names. The inclusion of over 155 new stereoselective and regioselective reagents or reactions including asymmetric syntheses, brings the total to over 540. Features that should be valuable to the reader include over 3000 references, a names index, reagent index, reaction index and a functional group transformation index. The latter of these indexes will allow the reader to search for conversions of one functional group to another and has proved a much utilized tool for the synthetic chemist, searching for pathways to perform synthetic procedures.

Autoren/Hrsg.

Stumer, C.

Hassner, Alfred

Baldwin, J E

Williams, Robert M

Weitere Mitwirkende

Baldwin, J.E.

Williams, Robert M.

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie Supramolekularchemie
• Wirtschaftswissenschaften Wirtschaftssektoren & Branchen Primärer Sektor Agrarökonomie, Ernährungswirtschaft
• Naturwissenschaften Agrarwissenschaften Agrarwissenschaften Landwirtschaftliche Bewässerung

Inhaltsverzeichnis

Halogenation reagent, Appel; crisscross cycloaddition, Bailey; iodination, Barluenga; deoxygenation, Barton-McCrombie; cycloaromatization, Bergman; rearrangement, Brandi-Guarna; heterocyclization, Buchwald; reducing agent, Chiatgilialoglu; heterocycle synthesis, G. Enders; olefin metathesis, Grubbs; asymmetric epoxidation, Jacobsen; asymemetric oxidation, Kagan-Modena; amine displacement, Katritzky; N-Acyl rearrangement, Kawase; zinc vinyl coupling, Knochel; hydroxycyclopropanation, Kulinkovich; oxidations, Nicolaou; aminoacid synthesis, O'Donnell; enone synthesis, Saegusa; catalytic nitrogenation, Shibasaki; chiral transfer, Yamamoto. (Part contents)