LES ALCYNES PDF

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Interactions des alcynes avec les complexes carbéniques du tungstène portant une double liaison carbone— carbone: Accès aux dérivés bicyclo[4,1,0]. Download Citation on ResearchGate | Réaction des halogenures de titane(IV) avec les alcynes: Formation d’halogénoalcènes | The behaviour of some mono-. Download Citation on ResearchGate | Action du chlorure de fer(III) sur les alcynes: Reduction du fer(III) en fer(II) et formation d’un chloro-alcene | The behaviour.

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CHIM 263 – Chimie organique II

You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: EP Kind code of ref document: In Chapter 5, a new way to control the enantioselectivity in 1,3-dipolar cycloaddition reactions is described.

The utility of this reaction alcynfs been extended to other products, including in situ reduction of the 2-pyrroline to pyrolidines, or oxidation to form alcyens. Methods of refining and producing dibasic esters and acids from natural oil feedstocks.

US USA1 en Outline Masquer le plan. Comparison of three enoate reductases and their potential use for biotransformations. Title Creator Subject Faculty Date. Catalysts for partial oxidation of hydrocarbons and method of partial oxidation of hydrocarbons. Houk et le Dr. Enzymatic processes for the production of 4-substituted 3-hydroxybutyric acid derivatives and vicinal cyano, hydroxy substituted carboxylic acid esters.

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Method for producing distillate from a hydrocarbon feed, comprising alcohol condensation. In addition, the results of the theoretical investigation of Chapter 2 are exploited to show how alcynex in the phosphorus substituents can be used to fine tune regioselectivity of alkyne cycloadditions without pes the substituents on the final product.

Record 1 of 1. The University’s open access institutional repository: Access to the text HTML. In addition, the reaction proceeds with high diastereo- and regioselectivity.

Importantly, these 1,3-dipoles display divergent regioselectivity, which can be exploited to synthesize a variety of pyrroles with high selectivity through the use of the appropriate reactant. Cycloaddition reactions of the above mentioned dipoles are examined with a range of unsymmetrical electron poor and electron rich alkynes, and by comparing the behavior of these related dipoles, trends are observed in regioselectivity that relates to the alkyne ionization potential.

Polycyclic 2-pyrrolines are generated in rapid cycloaddition reactions, in a modular fashion from easily accessible starting materials: Double catalytic addition of diazo compounds to alkynes: These 1,3-dipoles have been previously demonstrated to be accessible in a one-pot reaction of imines, acid chlorides and organophosphorus reagents, and participate in 1,3-dipolar cycloaddition reactions.

alcynse

Alkenes/Alkynes by Hatim Rhazi Filali on Prezi

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Cloning and nucleotide sequence of fosfomycin biosynthetic genes of Streptomyces wedmorensis. Propargylic carboxylates lead to conjugated dienes lfs coupling of the diazoalkane carbene with the alkyne terminal carbon and 1,2-shift of the carboxylate. Different phosphites and phosphonites are tested for their ability to mediate intramolecular cycloaddition with alkenes, and optimum results are obtained with 2-catechyl PPh.

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Access to the PDF text. A unique role in the addition of diazoalkane carbene to alkynes. Enantioselective reduction of carbonyl compounds by whole-cell biotransformation, combining a formate dehydrogenase and a R -specific alcohol dehydrogenase.

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Personal information regarding our website’s visitors, including their identity, alcyned confidential. X-ray crystallographic studies demonstrate the significant role of the PR3 unit on the ground state structure of these dipoles and their reactivity.

Molecular characterization of genes of Pseudomonas sp.

While each of the dipoles are established to participate in 1,3-dipolar cycloaddition led, until now, no general rules regarding the factors that control regioselectivity have been described.

Lea hydrolases from yeasts and other sources: Kind code of ref document: Direct route to alkenyl alkylidene bicyclohexane derivatives. The objective of the research described in this thesis is to both understand the reactivity of these dipoles, and exploit their cycloaddition with alkynes and alkenes to synthesize pyrroles and 2-pyrrolines with high regio- diastereo- and enantioselectivity. Contact Help Who are we? Substrate specificity and enantioselectivity of 4-hydroxyacetophenone monooxygenase.