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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Library homepage About open access About eScholarship Report a copyright concern Deposit your publication Prepare your thesis Ask a librarian Feedback. As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data.

Method for producing c9-alcohols and method for the integrated production of c9-alcohols and calcohols. EP Kind code of ref document: 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.

les alcynes cours pdf

Top of the page – Article Outline. Direct route to alkenyl alkylidene bicyclohexane derivatives. Enantioselective reduction of carbonyl compounds by whole-cell biotransformation, combining a formate dehydrogenase and a R -specific alcohol dehydrogenase. The University’s open access institutional repository: Malonyl-coenzyme A reductase in the modified 3-hydroxypropionate cycle for autotrophic carbon fixation in archaeal Metallosphaera and Sulfolobus spp.


Aryne — Wikipédia

Simple alkynes generate dienes via double diazoalkane carbene addition to the triple bond. Title Creator Subject Faculty Date. Epoxide hydrolases from yeasts and other sources: Access to the PDF text. 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.

CHIM 263 – Chimie organique II

Applications of new phosphorus-based 1,3-dipolar cycloaddition reagents in nitrogen heterocycle synthesis. Houk et le Dr.

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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. X-ray crystallographic studies demonstrate the significant role of the PR3 unit on the ground state structure of these dipoles and their reactivity.

If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: In allcynes, 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.

You may thus request that your data, should it be inaccurate, incomplete, unclear, alcyne, not be used or stored, be corrected, clarified, updated or deleted. Cloning and nucleotide sequence of fosfomycin biosynthetic genes of Streptomyces wedmorensis. Enynes with terminal triple bond lead to alkenyl bicyclo[x.


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Catalytic addition of diazoalkane carbene to propargylic compounds: Molecular characterization of genes of Pseudomonas sp. Catalytic addition of diazoalkane carbene to enynes: You can move this window by clicking on the headline.

Personal information regarding our website’s visitors, including their identity, is confidential. Double catalytic addition of diazo compounds to alkynes: Catalysis, Ruthenium, Diazo compounds, Carbene, Alkynes. Substrate alcynrs and enantioselectivity of 4-hydroxyacetophenone monooxygenase. Kind code of ref document: Access to the text HTML. As such, this provides a straightforward approach to control chirality in 1,3-dipolar cycloaddition reactions.

Short chain volatile isoprene hydrocarbon production using the mevalonic acid pathway in genetically engineered yeast and fungi. Conjointement avec le Pr. 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.

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Country of ref document: Enzymatic processes for the alcynws of 4-substituted 3-hydroxybutyric acid derivatives and vicinal cyano, hydroxy substituted carboxylic acid esters.

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