Reakcje rozszczepiania laktonów : zastosowanie w syntezie organicznej

Skiera, I.; Paryzek, Z.

Artykuł - szczegóły

Tytuł artykułu

Reakcje rozszczepiania laktonów : zastosowanie w syntezie organicznej

Autorzy

Skiera I. , Paryzek Z.

Wybrane pełne teksty z tego czasopisma

Identyfikatory

Warianty tytułu

The cleavage reactions of lactones : application in organic chemistry

Języki publikacji

Abstrakty

Lactones, being derivatives of hydroxy carboxylic acids, represent a special group of intramolecular esters. A large number of biologically important natural products are derivatives of chiral y- and 8-lactones. In addition, these commonly encountered compounds, due to their high reactivity, are valuable synthetic intermediates. Lactones are particularly susceptible to nucleophilic attack. As a consequence, the cleavage of the lactone ring is a commonly used process in laboratory synthesis of organic compounds and in industry. Cleavage of lactones may be effected under variety of reaction conditions including reagents, catalysts, solvents and temperature. The chemoselectivity observed in these reactions allows selective reactions of multifunctional compounds, very often of rather complicated structure. The enhanced reactivity of lactones toward nucleophiles makes hydrolysis their most investigated reaction. The ring cleavage occurs under basic (alkali metal hydroxides or alkoxides, tertiary amines) or acidic (Bronsted or Lewis acids) conditions. The effective cleavage of the lactone ring occurs also in reactions with nitrogen nucleophiles, which include ammonia, primary and secondary amines and hydrazine derivatives, as commonly used reagents. Sulphur and selenium derivatives are prepared in reactions of lactones with S- and Se-nucleophiles. The effective nucleophilic reducing agents include metal hydrides, of which lithium aluminium hydride is the most frequently used reagent. Other reducing agents like sodium borohydride and other complex boron hydrides have also been reported. Reductive cleavage of lactones under catalytic hydrogenation conditions and with the aid of complex reducing systems are discussed. The metaloorganic reagents effectively cleave lactones, while a new carbon-carbon bonds are formed. Since the literature concerning transformations of lactones is enormous, in this review the selected examples are included to demonstrate usefulness of lactone cleavage reactions for diverse synthetic purposes.

Słowa kluczowe

laktony reakcje rozszczepiania laktonów hydroliza laktonów redukcja laktonów

lactones lactone cleavage reactions lactone hydrolysis reduction of lactones

Wydawca

Polskie Towarzystwo Chemiczne

Czasopismo

Wiadomości Chemiczne

Rocznik

2004

Tom

[Z] 58, 11-12

Strony

845--879

Opis fizyczny

Bibliogr. 150 poz., schem.

Twórcy

autor

Skiera I.

Wydział Chemii, Uniwersytet im. A. Mickiewicza, ul Grunwaldzka 6, 60780 Poznań

autor

Paryzek Z.

Wydział Chemii, Uniwersytet im. A. Mickiewicza, ul Grunwaldzka 6, 60780 Poznań

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