Blanchot Mathieu (18 results)

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Taschenbuch. Condition: Neu. Regio- and Stereoselective Catalytic Addition of Amides to Alkynes | Synthesis of the enamide substructure in the most atom-economic and environmentally friendly way | Mathieu Blanchot | Taschenbuch | 228 S. | Englisch | 2015 | Südwestdeutscher Verlag für Hochschulschriften | EAN 9783838111124 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

8° , Broschiert. Condition: Gut. 94 Seiten, Einband mit leichten Gebrauchsspuren, Zustand gut Sprache: Deutsch Gewicht in Gramm: 1010.

Couverture rigide. Condition: Comme neuf. 2 volumes In-4 sous emboitage.

Condition: Used: Like New. LIVRE A L?ETAT DE NEUF. EXPEDIE SOUS 3 JOURS OUVRES. NUMERO DE SUIVI COMMUNIQUE AVANT ENVOI, EMBALLAGE RENFORCE. EAN:9782818968383.

Condition: Used: Like New. LIVRE A L?ETAT DE NEUF. EXPEDIE SOUS 3 JOURS OUVRES. NUMERO DE SUIVI COMMUNIQUE AVANT ENVOI, EMBALLAGE RENFORCE. EAN:9782818946992.

Condition: Used: Like New. LIVRE A L?ETAT DE NEUF. EXPEDIE SOUS 3 JOURS OUVRES. NUMERO DE SUIVI COMMUNIQUE AVANT ENVOI, EMBALLAGE RENFORCE. EAN:9782818935224.

Condition: Used: Like New. LIVRE A L?ETAT DE NEUF. EXPEDIE SOUS 3 JOURS OUVRES. NUMERO DE SUIVI COMMUNIQUE AVANT ENVOI, EMBALLAGE RENFORCE. EAN:9782818940846.

Condition: Used: Like New. LIVRE A L?ETAT DE NEUF. EXPEDIE SOUS 3 JOURS OUVRES. NUMERO DE SUIVI COMMUNIQUE AVANT ENVOI, EMBALLAGE RENFORCE. EAN:9782818996560.

Condition: Used: Like New. LIVRE A L?ETAT DE NEUF. EXPEDIE SOUS 3 JOURS OUVRES. NUMERO DE SUIVI COMMUNIQUE AVANT ENVOI, EMBALLAGE RENFORCE. EAN:9782818949788.

Condition: Used: Like New. Livre à l'état de neuf, très frais sans annotations ni défauts dissmulés.

Condition: Très bon. Merci, votre achat aide à financer des programmes de lutte contre l'illettrisme.

Couverture rigide. Condition: Très bon. Cycle complet en 4 volumes in-4, cartonnages couleurs. Quand la plus grande aventurière du XXe siècle dévoile ses secrets.

Dessin original signé, daté et titré à la mine de plomb 27 x 23 (motif). Portrait du peintre qui fut l'une des figures inspiratrices de cette remarquable artiste d'ici, trop tôt disparue, hélas jamais rencontrée et dont l'oeuvre crystallise cette notion de "littérArture" qui nous est chère. Fascinée par les écrivains, en sus de quelques peintres (Giacometti en restera la référence spirituelle par une certaine proximité graphique dans les dessins et les sculptures), elle en portraitisa plus d'un avec qui nous partageons quelque affinité de lecteur, dont Gustave Roud.Le dessin est présenté sous ingénieux étui-boîte de Jacques Menétrey , accompagné par l'ouvrage collectif consacré au sujet, tiré de la bibliothèque de l'auteur, ce qu'atteste sa signature sur la garde:- A Bram van Velde/Celui qui ne peut se servir de mots, Fata Morgana 1975. Broché 29 x 23, couverture or-ange à rabats avec titre imprimé en blanc. Le faux-titre précise "Celui qui ne peut se servir de mots", recense les contributions de Alechinsky, Asse, Beckett (plusieurs fois portraitisé par Loul), Blanchot, Bonnefoy, Butor, Coutin, Dotremont, Dupin, Esteban, Frémon, Gaspar, Hebey, Horovitz, Jabès, Juliet, Kurz, Laporte, Levinas, Mason, Mathieu, Messagier, Micha, Noël, Putman, Schneider, Starobinsky, Toreilles. L'un des 1'100 exemplaires de l'édition originale courante sur Vergé, après 100 Arches avec suite signée des lithographies. > En cas de problème de commande, veuillez nous contacter par notre page d'accueil / If you have any problems with your order please contact us via our homepage <.

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The enamide moiety is an important substructure often encountered in biologically active compounds and synthetic drugs. Furthermore, enamides and their derivatives are versatile synthetic intermediates for polymerization, [4+2] cycloaddition, crosscoupling, Heck-olefinination, Halogenation, enantioselective addition or asymmetric hydrogenation. Traditional syntheses of this important substrate class involve rather harsh reaction conditions such as high temperatures and/or the use of strong bases. Based on previous work on the addition of secondary amides to alkynes, a new broadly applicable protocol for the catalytic addition of N-nucleophiles such as primary amides, imides and thioamides to terminal alkynes was developed. The choice of ligands and additives determines the regiochemical outcome so that with two complementary catalyst systems, both the E-anti-Markovnikov products and the Z-anti-Markovnikov products can be synthesized highly regio- and stereoselectively. 228 pp. Deutsch.

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. The enamide moiety is an important substructure often encountered in biologically active compounds and synthetic drugs. Furthermore, enamides and their derivatives are versatile synthetic intermediates for polymerization, [4+2] cycloaddition, crosscoupling,.

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The enamide moiety is an important substructure often encountered in biologically active compounds and synthetic drugs. Furthermore, enamides and their derivatives are versatile synthetic intermediates for polymerization, [4+2] cycloaddition, crosscoupling, Heck-olefinination, Halogenation, enantioselective addition or asymmetric hydrogenation. Traditional syntheses of this important substrate class involve rather harsh reaction conditions such as high temperatures and/or the use of strong bases. Based on previous work on the addition of secondary amides to alkynes, a new broadly applicable protocol for the catalytic addition of N-nucleophiles such as primary amides, imides and thioamides to terminal alkynes was developed. The choice of ligands and additives determines the regiochemical outcome so that with two complementary catalyst systems, both the E-anti-Markovnikov products and the Z-anti-Markovnikov products can be synthesized highly regio- and stereoselectively.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 228 pp. Englisch.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The enamide moiety is an important substructure often encountered in biologically active compounds and synthetic drugs. Furthermore, enamides and their derivatives are versatile synthetic intermediates for polymerization, [4+2] cycloaddition, crosscoupling, Heck-olefinination, Halogenation, enantioselective addition or asymmetric hydrogenation. Traditional syntheses of this important substrate class involve rather harsh reaction conditions such as high temperatures and/or the use of strong bases. Based on previous work on the addition of secondary amides to alkynes, a new broadly applicable protocol for the catalytic addition of N-nucleophiles such as primary amides, imides and thioamides to terminal alkynes was developed. The choice of ligands and additives determines the regiochemical outcome so that with two complementary catalyst systems, both the E-anti-Markovnikov products and the Z-anti-Markovnikov products can be synthesized highly regio- and stereoselectively.