Lygin (9 results)

Hardcover. Condition: Near Fine EX-LIBRARY copy. Dust Jacket Condition: No jacket. First Edition. London & New York:: Academic Press, 1966. A bright, clean, square, tight copy. Sharp corners. Stamped "WITHDRAWN" on the endpapers. Pages are unmarked. No underlining. No highlighting. No margin notes. Illustrated with many figures and diagrams. Graphs. Tables. Supplementary chapters by A. V. Kiselev & V. I. Lygin. Bibliographical references. Author Index. Subject Index. Bound in the original orange cloth with a green spine panel, lettered in shiny gold. . First Edition. Hard Cover. Near Fine EX-LIBRARY copy./No jacket. 8vo. xii, 428pp.

Taschenbuch. Condition: Neu. Novel Syntheses of Nitrogen Heterocycles from Isocyanides | Alexander Lygin | Taschenbuch | 200 S. | Englisch | 2015 | Südwestdeutscher Verlag für Hochschulschriften | EAN 9783838117546 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

Hardcover. Condition: sehr gut. Originalpappband, 207 Seiten, 22 cm x 14,9 cm, Glanzfolie am Rücken teilweise gelöst, Rückenkanten abgeschabt, so sehr gutes Exemplar Mit 92 Bildern, 25 Tafeln und 7 Schemata in deutscher Sprache.

Hardcover. 207 S. Guter Zustand. Die Leseseiten sind sauber und ohne Markierungen. Leichte Lager- und Gebrauchsspuren. Buch ist foliert (Umschlag aus selbstklebender Folie). Ausgeschiedenes Bibliotheksexemplar mit entsprechender Kennzeichnung. Ansonsten ordentliches Exemplar. 9783527258079 Sprache: Deutsch Gewicht in Gramm: 1000.

Hardcover. Condition: Good. In Russian. Lygin, Semyon Alexandrovich. Commodity-monetary relations under socialism. Saratov: Publishing House of Saratov, 1974. All images are for identification of editions only. Several books of the same edition may be available. Please feel free to request photos of available books.SKU7160913.

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The direct copper(I)-catalyzed synthesis of oligosubstituted pyrroles from substituted methyl isocyanides and acceptor-substituted acetylenes as well as copper(I)-mediated route to pyrroles from substituted methyl isocyanides and non-activated terminal acetylenes have been investigated. 2-Substituted phenyl isocyanides were obtained by trapping of generated in situ ortho-lithiophenyl isocyanide with electrophiles. This strategy has been effectively employed for the new synthesis of substituted 3H-quinazolin-4-ones (-thiones) including the naturally occurring alkaloids deoxyvasicinone and tryptanthrine. The reactions of ortho-lithiophenyl isocyanide and other ortho-lithiohetaryl isocyanides with aldehydes, ketones, and carbon dioxide have been investigated in detail. Two novel rearrangements of the intermediate 2-lithio-4H-3,1-benzoxazines have been disclosed. A novel copper-catalyzed synthesis of benzimidazoles from ortho-bromoaryl isocyanides and primary amines has been developed. 200 pp. Englisch.

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Lygin AlexanderAlexander V. Lygin was born in 1984 in Krasnokamensk, Russia. He studied chemistry at the M.V. Lomonosov Moscow State University in 2001-2006. Later he carried out his doctoral thesis work in the group of Prof. Armin d.

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The direct copper(I)-catalyzed synthesis of oligosubstituted pyrroles from substituted methyl isocyanides and acceptor-substituted acetylenes as well as copper(I)-mediated route to pyrroles from substituted methyl isocyanides and non-activated terminal acetylenes have been investigated. 2-Substituted phenyl isocyanides were obtained by trapping of generated in situ ortho-lithiophenyl isocyanide with electrophiles. This strategy has been effectively employed for the new synthesis of substituted 3H-quinazolin-4-ones (-thiones) including the naturally occurring alkaloids deoxyvasicinone and tryptanthrine. The reactions of ortho-lithiophenyl isocyanide and other ortho-lithiohetaryl isocyanides with aldehydes, ketones, and carbon dioxide have been investigated in detail. Two novel rearrangements of the intermediate 2-lithio-4H-3,1-benzoxazines have been disclosed. A novel copper-catalyzed synthesis of benzimidazoles from ortho-bromoaryl isocyanides and primary amines has been developed.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 200 pp. Englisch.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The direct copper(I)-catalyzed synthesis of oligosubstituted pyrroles from substituted methyl isocyanides and acceptor-substituted acetylenes as well as copper(I)-mediated route to pyrroles from substituted methyl isocyanides and non-activated terminal acetylenes have been investigated. 2-Substituted phenyl isocyanides were obtained by trapping of generated in situ ortho-lithiophenyl isocyanide with electrophiles. This strategy has been effectively employed for the new synthesis of substituted 3H-quinazolin-4-ones (-thiones) including the naturally occurring alkaloids deoxyvasicinone and tryptanthrine. The reactions of ortho-lithiophenyl isocyanide and other ortho-lithiohetaryl isocyanides with aldehydes, ketones, and carbon dioxide have been investigated in detail. Two novel rearrangements of the intermediate 2-lithio-4H-3,1-benzoxazines have been disclosed. A novel copper-catalyzed synthesis of benzimidazoles from ortho-bromoaryl isocyanides and primary amines has been developed.