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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Malonyl-coenzyme A reductase in the modified 3-hydroxypropionate cycle for autotrophic carbon fixation in archaeal Metallosphaera and Sulfolobus spp. Houk et le Dr. All items in eScholarship McGill are protected by copyright with all rights reserved unless otherwise indicated.

Alkenes/Alkynes by Hatim Rhazi Filali on Prezi

Simple alkynes generate dienes via double diazoalkane carbene addition to the triple bond. Catalytic addition of diazoalkane carbene to enynes: 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.

Cloning and nucleotide sequence of fosfomycin biosynthetic genes of Streptomyces wedmorensis. Enzymatic processes for the production of 4-substituted 3-hydroxybutyric acid derivatives and vicinal cyano, hydroxy substituted carboxylic acid esters.

Previous Article Gecom-Concoord Access to the full alccynes of this article requires a subscription. Country of ref document: Epoxide hydrolases from yeasts and other sources: A unique role in the addition of diazoalkane carbene to alkynes. Method for producing distillate from a hydrocarbon feed, comprising alcohol condensation. Personal information regarding our website’s visitors, including their identity, is confidential.

Enynes with terminal triple bond lead to alkenyl bicyclo[x. The utility of this reaction has been extended to other products, including in situ reduction of the 2-pyrroline to pyrolidines, or oxidation to form pyrroles. Journal page Archives Contents list. Deposit your publication Prepare your thesis Ask a librarian Feedback.

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Cycloaddition reactions of the above mentioned dipoles are examined with a alcunes 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.

Methods of refining and producing dibasic esters and acids from natural acynes feedstocks. Record 1 of 1. The University’s open access institutional repository: Enantioselective reduction of carbonyl compounds by whole-cell alcyne, combining a formate dehydrogenase and a R -specific alcohol dehydrogenase.

In addition, the reaction proceeds with high diastereo- and regioselectivity. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Substrate specificity and enantioselectivity of 4-hydroxyacetophenone monooxygenase. US USA1 en Different phosphites and phosphonites are tested for their ability to mediate intramolecular cycloaddition with alkenes, and optimum results are obtained with 2-catechyl PPh.

As such, this provides a straightforward approach to control alcnes in 1,3-dipolar cycloaddition reactions.

Comparison of three enoate reductases and their potential use for biotransformations. X-ray crystallographic studies demonstrate the significant role of the PR3 unit on the ground state structure of these dipoles and their reactivity.

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. Contact Help Who are we? In addition, the results of the theoretical investigation of Chapter 2 are exploited to show how changes in the phosphorus substituents can be used to fine tune regioselectivity of alkyne cycloadditions without modifying the substituents on the final product. While each of the dipoles are established to participate in 1,3-dipolar cycloaddition reactions, until now, no general rules regarding the factors that control regioselectivity have been described.

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Conjointement avec le Pr. In Chapter 5, a new way to control the enantioselectivity in 1,3-dipolar cycloaddition reactions is described. Title Creator Subject Faculty Date. Top of the page – Article Outline. Polycyclic 2-pyrrolines are generated in rapid cycloaddition reactions, in a modular fashion from easily accessible starting materials: In conjunction with Prof.

Access to the PDF text. 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.

You can move this window by clicking on the headline. Catalysts alchnes partial oxidation of hydrocarbons and method of partial oxidation of hydrocarbons. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties. Outline Masquer le plan.

Short chain volatile isoprene hydrocarbon production using the mevalonic acid alcyes in genetically engineered yeast and fungi.

Propargylic carboxylates lead to conjugated dienes by coupling of the diazoalkane carbene with the alkyne terminal carbon and 1,2-shift of the carboxylate. Double catalytic addition of diazo compounds to alkynes: Direct route to alkenyl alkylidene bicyclohexane derivatives.

Catalytic addition of diazoalkane carbene to propargylic compounds: Molecular characterization of genes of Pseudomonas sp.

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