Allyl sulfides reactive substrates for olefin metathesis pdf

Olefin metathesis reactions of sulfurcontaining alkenes and. Onprotein reaction kinetics reveal a rapid reaction with rate constants of seacmediatedcm comparable. However, the unique reactivity of allyl sulfide in. Olefin metathesis reactions of sulfur containing alkenes and. The name is derived from the latin word for garlic, allium sativum. Allyl selenides are superior metathesis substrates to allyl sulfides in aqueous cross metathesis.

A profile of catalyst activity is described, along with the first demonstration of allyl sulphides as traceless promoters in relayed ringclosing metathesis. Letter synthesis of vinyl and allylphosphonates by olefin cross metathesis 1037. Allyl sulphides are reactive substrates in rutheniumcatalysed olefin metathesis reactions, provided each substrate is matched with a suitable catalyst. Additional allylic sulfone substrates were evaluated to assess the scope of this surprising reaction and to. Acetic acid and 1,4benzoquinone did not reduce the catalyst activity.

For example, allyl sulfides, including diallyl sulfide, is one of the reactive substrates for olefin metathesis reaction a chemical. Olefin metathesis ruthenium and molybdenium based precatalysis. Allyl sulfides undergo efficient cross metathesis in aqueous media with hoveydagrubbs second generation catalyst 1. Synthesis of biologically active dicarba analogues of the peptide hormone oxytocin using ringclosing metathesis. This led to a new benchmark in substrate complexity for cross metathesis and expanded the potential of olefin metathesis for other applications in chemical biology. The fact that catalyst 1 tolerates olefins substituted with an allylic sulfide suggested that other functional groups that could behave as ligands for ruthenium might be viable substrates. The high reactivity of allyl sulfides in cross metathesis was exploited in the first examples of cross metathesis on a protein surface. Olefin metathesis reactions of sulfur containing alkenes. Depending on the substrate and reaction conditions, it may prove more effective than 682284.

Olefin metathesis in water at room temperature using tpgs. The fact that catalyst 1 tolerates olefins substituted with an allylic sulfide. Olefin cross metathesis is a particularly powerful transformation that has been exploited extensively for the formation of complex products. Functional group diversity by ruthenium catalyzed olefin. The metathesis of unsaturated oleochemicals is an excellent tool for generating. Synthesis of vinyl and allylphosphonates by olefin cross. The high reactivity of allyl sulfides in cross metathesis was exploited in the. Allyl sulfides are privileged substrates in olefin metathesis. The investigation of palladiumcatalyzed alkoxyallylation of activated olefins, followed by ringclosing metathesis to synthesize functionalized sevenmembered ring allyl ethers is described.

The high reactivity of allyl sulfides in olefin metathesis is remarkable, given that many sulfurcontaining substrates are incompatible with rutheniumbased olefin metathesis catalysts. Ringopening metathesis polymerization, oxidative coupling, electrochemical polymerization, case study. Except for the poorly watersoluble octyl allyl sulfide 11, moderate to high product conversions 3586% were achieved for the reactions with other alkylsubstituted allyl sulfides 22, 24, which further supports the broad substrate scope of mbl29s,h64v,v68f. This chapter will focus only on cross metathesis cm and how substrate substitution affects the distribution of products. Imparting functional variety to cellulose ethers via. Developing strategies for sitespecific protein modifications is an ongoing challenge in chemical biology. Olefin metathesis has emerged as a powerful tool in organic synthesis. Herein, the concept of multiple olefin metathesis polymerizations momp is introduced where two or three. For their elucidation of the reaction mechanism and. Oct 14, 2009 olefin isomerizationmigration can be an annoying side reaction of olefin metathesis, in no small part because the side products are usually difficult to separate from the desired product.

It is a colourless liquid with a strong odor characteristic of alkyl sulfides. The allylic chalcogen effect in olefin metathesis core. Olefin metathesis for siteselective protein modification yuya a. Recently, the discovery of the rate enhancement by allyl sulfides in aqueous cross metathesis has allowed the first examples of such a reaction on proteins. Allyl sulfides are priviledged substrates in aqueous olefin cross metathesis. Allyl sulfides undergo efficient cross metathesis in aqueous media with hoveyda. The activating effect of an allylic hydroxy group in metathesis has been known for more than 10 years, and many organic.

Allyl sulfides are privileged substrates in aqueous crossmetathesis. Olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes olefins by the scission and regeneration of carboncarbon double bonds. The high reactivity of allyl sulfides in crossmetathesis was exploited in the first examples of crossmetathesis on a protein surface. This led to a new benchmark in substrate complexity for cross metathesis and expanded the potential of olefin metathesis for other applications in chemical. The effect of allylic hydroxy groups in olefin metathesis the activating effect of allylic hydroxy groups in ringclosing metathesis rcm was first identified by hoye. Lin ya1, chalker jm, floyd n, bernardes gj, davis bg. In stark contrast, allyl sulfides actually enhance the rate of metathesis in comparison with other alkenes, when matched. Olefin metathesis is now a wellentrenched synthetic technique, and is a powerful method for the clean construction of innumerable classes of chemical architectures.

The design and elaboration of a series of macrocyclic templates that exhibit a propensity to adopt a strand. Alkene metathesis, also known as olefin metathesis, was the subject of the 2005 nobel prize in chemistry. Olefin metathesis has become a mainstay in organic synthesis. Chauvin was the first to produce a viable mechanism for olefin metathesis. In the presence of certain transitionmetal compounds, including various metal carbenes, olefins exchange the groups around the double bonds, resulting in several outcomes. Olefin metathesis reactions of sulfurcontaining alkenes. Olefin metathesis in water at room temperature using tpgs750m description tpgs750m, dl. The allylic chalcogen effect in olefin metathesis open.

Allyl sulfides have gained traction in recent years as promoters for olefin metathesis. The complex 3 is less reactive than the parent 2 at rt for rcm. In an extreme case, the reaction of allyl diphenylphosphine with 5 mol% 1 failed to produce any of the desired cross metathesis adduct and returned terminal olefin unreacted. Cm reaction selective for the heterocoupled product and the eisomer. Olefin metathesis in organic synthesis wendy jen macmillan group meeting january 17, 2001. The metathesis reaction mechanism, proposed by chauvin in 1971, suggests that the reaction proceeds via the reversible formation of a metallacyclobutane intermediate scheme 2, intermediates ii and iv. Olefin metathesis welldefined ru catalysts 3rd literature seminar august 5, 20 soichi ito m2 1 topics introduction evolution of ruthenium catalysts from illdefined catalysts to welldefined catalysts illdefined ruthenium catalysts. Jul 30, 2008 allyl sulfides are privileged substrates in aqueous cross metathesis. Because of the relative simplicity of olefin metathesis, it often creates fewer undesired byproducts and hazardous wastes than alternative organic reactions. Metathesis catalysts eyal tzur department of chemistry, ben. Davisa introduction chemical modification of proteins is a powerful method for study and modulation of macromolecular function.

Allyl selenides were exceptionally reactive olefin metathesis substrates, enabling a broad range of protein modifications not previously possible. Lewis acid additives in cm of sulfide 12 and allyl alcohol 2 s23. This article describes the cross metathesis of allyl acetate and cis1,4diacetoxy2butene with methyl 10undecenoate and methyl oleate, which are oleochemical key substrates. The high reactivity of allyl sulfides in olefin metathesis is remarkable, given that many sulfurcontaining substrates are incompatible with. Olefin metathesis college of saint benedict and saint. Olefin metathesis, or alkene metathesis, is an important process in petroleum refining and in the synthesis of important compounds such as pharmaceuticals. Microwaveaccelerated crossmetathesis reactions of n. Relatively intolerant of protons on heteroatoms rcooh. The enhanced reactivity of allyl sulfide, along with earlier reports of a similar effect by allylic hydroxy. Allyl sulfides undergo efficient crossmetathesis in aqueous media with hoveyda.

In other words, it occurs through the concerted interaction of one. Based on our results on allyl sulfides, alongside reports on the activating effect of allylic alcohols and ethers, the positive influence of allyl chalcogens on the rate of olefin metathesis is obvious. Starting from commercially available ethyl cellulose, terminally unsaturated alkyl groups were appended as metathesis handles by reaction with allyl chloride, 5bromo1pentene, 7bromo1heptene and 11. Common uses of episulfides in both academic and industrial settings most often involve their use as monomers in polymerization reactions. The reaction mixture was stirred and heated in a water bath to. In the preliminary work, allyl sulfides were found to be reactive substrates in aqueous cross metathesis cm enabling the first examples of protein modification via this approach. Tocopherol methoxypolyethylene glycol succinate, is a designer surfactant composed of a lipophilic. Olefin metathesis for siteselective protein modification. Regio and enantioselective iridiumcatalyzed allylation. A range of metathesis substrates containing different olefin tether of various lengths were screened. The olefin metathesis reaction harvard web publishing.

Grubbs arnold and mabel beckman laboratories of chemical synthesis, division of chemistry and chemical engineering, california institu te of technology, pasadena, california 91125, usa email. Olefin metathesis welldefined ru catalysts 3rd literature seminar august 5, 20 soichi ito m2 1. Through literature research, the activation effect of allylic chalcogens in olefin metathesis appears to be a general phenomenon. Olefin metathesis for siteselective protein modification yuya angel lin st. In this article the reactivity of sulfides, sulfones and sulfoxides in olefin metathesis reactions is discussed. The reaction involves the rearrangement of carboncarbon double bonds, through the use of metal catalysts, such as the grubbs ru catalyst, schrock w, mo, and re catalysts, and titanocenebased catalysts. Must be handled under ar or n2 using dry solvents and substrates. Prevention of undesirable isomerization during olefin metathesis. Selective cross metathesis with ruthenium catalysts. Page 71 olefin metathesis reactions of sulfurcontaining alkenes and dienes cezary samojowicz and karol grela institute of organic chemistry, polish academy of sciences, kasprzaka 4452, 01224 warsaw, poland email. Remarkable acceleration of the cross metathesis reaction minutes compared to hours over conventional reflux heating was observed.

Olefin metathesis reactions of sulfur containing molecules arkivoc. Episulfides have an innate ring strain due to the nature of threemembered rings. The principles considered in this report are important not only for expanding the repertoire of bioconjugation but also for the application of olefin metathesis in general synthetic endeavors. Carbonyl olefin metathesis michigan state university. Olefin metathesis is a popular and useful reaction. Inhibiting olefin isomerization all things metathesis. Rutheniumcatalyzed olefin crossmetathesis tolerates a wide range of functional.

Olefin metathesis 3 2005 the nobel prize in chemistry yves chauvin prize share. Diallyl sulfide has known to possess high chemical activities. Microwaveaccelerated cross metathesis reactions of n. Allyl methyl sulfide is an organosulfur compound with the chemical formula ch 2 chch 2 sch 3. A profile of catalyst activity is described, along with the first demonstration of allyl sulphides as traceless promoters in relayed ringclosing metathesis reactions. Ziolkowski in recognition of his significant contribution to homogeneous catalysis and coordination chemistry. Australian journal of chemistry an international journal for chemical science publishes research papers from all fields of chemical science. The olefin metathesis reaction was reported as early as 1955 in a tiiicatalyzed. Therefore, most reactions of episulfides involve ringopening. Profluorescent substrates for the screening of olefin. Apparently, the exceptional reactivity of 1 toward olefins 12 exceeds its reac. By reducing the steric hindrance around the allyl sulfide on protein surface through a chemical spacer, the rate and conversion of metathesis reaction on proteins was greatly enhanced.

Cross metathesis cm has recently emerged as a viable strategy for protein modification. Synthesis of biologically active dicarba analogues of the. The influence of the olefin substituents on the diastereoselectivity of the alkoxyallylation has also been examined. Schrock accidently created first stable metal carbene catalyst at mit. Please consult the safety data sheet for information regarding hazards and safe handling practices.

Allyl sulfides have emerged as useful promoters for olefin metathesis. Several sulfurcontaining alkenes have been applied as substrates in olefin metathesis reactions. In 1844, theodor wertheim isolated an allyl derivative from garlic oil and named it schwefelallyl. To date, there has been no report on a metathesis polymerization utilizing more than one metathesis process. Covalent attachment of fluorescent probes, for example, allows proteins to be tracked both in vitro and in vivo. Molecular modeling, synthesis, and biological evaluation of. In order to overcome this limitation and prepare zolefins via metathesis, chemists have adopted two strategies. Comparison of reactivity in the cross metathesis of allyl. Grubbs gave synthetic chemists an air stable and watersoluble metal carbene. Potential for isomerization of olefin if catalyst is not reactive enough o o oh oh o o oh oh o o oh oh o o. Apparently the olefin electron density of allyl alcohols is su. Application to siteselective protein modification yuya a. Microwave heating has been utilised for the cross metathesis reaction of n allyl amino acid substrates to generate olefin homodimers.

Sallylcysteine was incorporated chemically into the protein, providing the requisite allyl sulfide handle. Ruthenium catalyzed crossmetathesis versus silylative coupling of vinyl and allyl sulfides with vinylsilanes the paper is dedicated to professor jozef j. Siteselective protein modification has become an important tool to study protein functions in chemical biology. Prevention of undesirable isomerization during olefin. Rapid crossmetathesis for reversible protein modifications. Allyl sulfides are priviledged substrates in aqueous. In stark contrast, allyl sulfides actually enhance the rate of metathesis in comparison with other alkenes, when. Chapter 6 zselective ruthenium metathesis catalysts. Olefin metathesis olefin metathesis, or alkene metathesis, is an important process in petroleum refining and in the synthesis of important compounds such as pharmaceuticals. Because of the relative simplicity of olefin metathesis, it often creates fewer undesired byproducts and hazardous wastes than alternative. An allyl group is a substituent with the structural formula h 2 cch. Allyl sulfides are privileged substrates in aqueous cross metathesis. The synthesis of highly functionalized sevenmembered allyl. The molecule features two functional groups, an allyl ch 2 chch 2 and a sulfide.

The allyl sulfide 1 c was also converted to the cross. Pdf the allylic chalcogen effect in olefin metathesis. Allyl sulfides are privileged substrates in aqueous cross. Ruthenium catalyzed cross metathesis versus silylative coupling of vinyl and allyl sulfides with vinylsilanes. Several sulfurcontaining alkenes have been applied as substrates in olefin. Functional group diversity by ruthenium catalyzed olefin cross. The isomerization is catalyzed by metal hydride species formed in the decomposition of the catalyst see schmidt, eur. One strategy relies on the use of specially designed substrates that yield zolefins upon metathesis and. Olefin crossmetathesis, a mild, modular approach to. However, these molecules are valuable in organic synthesis. Synthesis of vinyl and allylphosphonates by olefin cross metathesis arnab k. The first generation ruthenium precatalysts, such as 1a are known to be.

The olefin metathesis reaction of sulfurcontaining olefins is a challenging transformation. In total synthesis in 2011, olefin metathesis was used for times. Alternatively, if the cross partner is more reactive versus cyclic olefin, the major product arises from homocoupling cross. Synthesis of vinyl and allylphosphonates by olefin crossmetathesis arnab k. Ruthenium catalyzed crossmetathesis versus silylative. Mechanism of olefin metathesis exchange double bonds. Abstract siteselective protein modification has become an important tool to study protein functions in chemical biology. Cross metathesis is a powerful method for the rapid synthesis of simple and complex olefinic building blocks, and an excellent model has been developed by grubbs to predict the outcome of cross metathesis reactions, based upon reactant olefin type i. The allylic chalcogen effect in olefin metathesis beilstein journals. Relatively intolerant of protons on heteroatoms rcooh, rsh, roh, etc.

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