2-alkene-1,5-diol epoxide

Diols generally react with dichlorocarbene to produce a mixture of alkenes and chlorinated cyclopropanes or chloroalkanes, depending on the reaction conditions whereas, under phase-transfer catalysed conditions, the major products are the alkenes and epoxides produced by ring closure of the initial adduct (Scheme 7.20) [14]. When an excess of chloroform is used, further reaction of the alkenes with dichlorocarbene produces the cycloadducts. In addition to the formation of the alkene and epoxide, 1,2-dihydroxycyclooctane yields cyclooctanone, via a 1,2-hydride shift within the intermediate carbenium ion. 

Diol epoxides, a very special and highly reactive subclass of alkene oxides encountered in the metabolism of polycyclic aromatic hydrocarbons. 

This chapter begins, thus, with a short introduction to the chemical reactivity of epoxides. We continue with a description of the epoxides hydrolases and their biochemistry, and devote most of its length to a systematic discussion of the substrates hydrated by these enzymes. Arene oxides and diol epoxides will be presented first, followed by a large variety of alkene and cy-cloalkene oxides. 

Molybdenum and tungsten compounds have long been known to catalyze the transformations of alkenes into epoxides and diols by hydrogen peroxide.171"173 This reaction was found to be suitable for the epoxidation of water-soluble alkenes such as allylic alcohols (equation 30)174,175 or unsaturated carboxylic acids (equation 31).171 Tungsten catalysts were found to be more active and selective in aqueous solution than molybdenum complexes. 

The development of simple systems that allow for the asymmetric oxidation of allyl alcohols and simple alkenes to epoxides or 1,2-diols has had a great impact on synthetic methodology because it allows for the introduction of functionality with concurrent formation of one or two stereogenic centers. This functionality can then be used for subsequent reactions that usually fall into the... 

Recently, comprehensive World Wide Web (Internet) databases have been established on insect pheromones and semiochemicals The Pherolist , a database of chemicals identified from sex pheromone glands of female lepidopteran insects and other chemicals attractive to male moths (Am et al., 1999) and The Pherobase , a database of pheromones and semiochemicals for Lepidoptera and other insect orders (El-Sayed, 2006). These large databases on behavior modifying chemicals have extensive cross-linkages for animal taxa, indexes of compounds and source (reference) indexes. The indexes include those compounds cited in this chapter and many more with pheromone and semiochemical function acetate esters, diols, epoxides, ethers, ketones and secondary alcohols. For example, The Pherolist reports approximately 90 epoxy derivatives of C17-C23 of n-alkancs, mono-alkenes and di-alkenes as insect semiochemicals. 

The relevant literature in this subfield is too voluminous to be detailed here. Overviews are available [62], and only a few recent references to the newest publications are given below. Oxidations of the following types have been performed alcohol - ketone [63] aldehyde —> acid alkene —> diol or epoxide [64-67] al-kene - aldehyde, acid 1-alkyne —> ketoaldehyde and acid (1 C-atom shorter) internal alkyne —> a,/3-epoxyketone vic-diol —> 1,2-diketone [68] or hydroxyketone [69] amine —> amine oxide [70] aromatic amine —> nitrosobenzene, nitrobenzene, azoxybenzene [71]. 

Since its discovery in 1991, methyltrioxorhenium (MTO, 80) has attracted much interest as one of the most versatile catalysts for oxidation.When it is associated with a stoichiometric amount of H2O2, the system can efficiently transform alkene to epoxide, although formation of undesired diol can occur. Alternatively, water-free conditions, using urea hydrogen peroxide (UHP), allow the formation of the desired epoxide without byproducts. A maj or drawback of the MTO/UHP system is its insolubility in organic solvents, leading to a kinetically slow heterogeneous system. 

Hydroxyl groups also participate as nucleophiles in a variety of other acid-catalyzed cyclizations of synthetic utility. One example is the Ritter reaction, which normally produces amides upon reaction of olefins or alcohols with nitriles. Cyclization occurs with 1,3-diols, hydroxy alkenes, or epoxides. Examples of each are given in Eqs. (74)-(76). 

Ca.ta.lysts, A small amount of quinoline promotes the formation of rigid foams (qv) from diols and unsaturated dicarboxyhc acids (100). Acrolein and methacrolein 1,4-addition polymerisation is catalysed by lithium complexes of quinoline (101). Organic bases, including quinoline, promote the dehydrogenation of unbranched alkanes to unbranched alkenes using platinum on sodium mordenite (102). The peracetic acid epoxidation of a wide range of alkenes is catalysed by 8-hydroxyquinoline (103). Hydroformylation catalysts have been improved using 2-quinolone [59-31-4] (104) (see Catalysis). 

Nucleophilic opening of oxiranes to give ultimately 1,2-diols is usually effected without isolation of the oxirane oxiranation (epoxidation) of alkenes with unbuffered peroxy-ethanoic acid or hydrogen peroxide in methanoic acid (Section 5.05.4.2.2(/)) tends to give monoesters of 1,2-diols (e.g. 53), which can be hydrolyzed to the diols (Scheme 46). 

Alkenes are reduced by addition of H2 in the presence of a catalyst such as platinum or palladium to yield alkanes, a process called catalytic hydrogenation. Alkenes are also oxidized by reaction with a peroxyacid to give epoxides, which can be converted into lTans-l,2-diols by acid-catalyzed epoxide hydrolysis. The corresponding cis-l,2-diols can be made directly from alkenes by hydroxylation with 0s04. Alkenes can also be cleaved to produce carbonyl compounds by reaction with ozone, followed by reduction with zinc metal. 

From what alkene was the following 1,2-diol made, and what method was used, epoxide hydrolysis or Os04 ... 

Diols can be prepared either by direct hydroxylation of an alkene with 0s04 followed by reduction with NaHSOj or by acid-catalyzed hydrolysis of an epoxide (Section 7.8). The 0s04 reaction occurs with syn stereochemistry to give a cis diol, and epoxide opening occurs with anti stereochemistry to give a trans diol. 

When asymmetric epoxidation of a diene is not feasible, an indirect route based on asymmetric dihydroxylation can be employed. The alkene is converted into the corresponding syn-diol with high enantioselectivity, and the diol is subsequently transformed into the corresponding trans-epoxide in a high-yielding one-pot procedure (Scheme 9.5) [20]. No cpirricrizalion occurs, and the procedure has successfully been applied to natural product syntheses when direct epoxidation strategies have failed [21]. Alternative methods for conversion of vicinal diols into epoxides have also been reported [22, 23]. 

In addition, also nonheme iron catalysts containing BPMEN 1 and TPA 2 as ligands are known to activate hydrogen peroxide for the epoxidation of olefins (Scheme 1) [20-26]. More recently, especially Que and coworkers were able to improve the catalyst productivity to nearly quantitative conversion of the alkene by using an acetonitrile/acetic acid solution [27-29]. The carboxylic acid is required to increase the efficiency of the reaction and the epoxide/diol product ratio. The competitive dihydroxylation reaction suggested the participation of different active species in these oxidations (Scheme 2). 

Heteropoly acids can be synergistically combined with phase-transfer catalysis in the so-called Ishii-Venturello chemistry for oxidation reactions such as oxidation of alcohols, allyl alcohols, alkenes, alkynes, P-unsaturated acids, vic-diols, phenol, and amines with hydrogen peroxide (Mizuno et al., 1994). Recent examples include the epoxidations of alkyl undecylenates (Yadav and Satoskar, 1997) and. styrene (Yadav and Pujari, 2000). 

The location of the position of double bonds in alkenes or similar compounds is a difficult process when only very small amounts of sample are available [712,713]. Hass spectrometry is often unsuited for this purpose unless the position of the double bond is fixed by derivatization. Oxidation of the double bond to either an ozonide or cis-diol, or formation of a methoxy or epoxide derivative, can be carried out on micrograms to nanograms of sample [713-716]. Single peaks can be trapped in a cooled section of a capillary tube and derivatized within the trap for reinjection. Ozonolysis is simple to carry out and occurs sufficiently rapidly that reaction temperatures of -70 C are common [436,705,707,713-717]. Several micro-ozonolysis. apparatuses are commercially available or can be readily assembled in the laboratory using standard equipment and a Tesla coil (vacuum tester) to generate the ozone. Reaction yields of ozonolysis products are typically 70 to 95t, although structures such as... 

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