Kwas winowy i jego pochodne we współczesnej chemii organicznej

Grajewski, J.

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Tytuł artykułu

Kwas winowy i jego pochodne we współczesnej chemii organicznej

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Grajewski J.

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Warianty tytułu

Tartaric acid and its derivatives in current organic chemistry

Języki publikacji

Abstrakty

The tartaric acid and its salts have been present in chemistry for almost 350 years, since Pierre Seignette isolated Rochelle salt in 1675. Since that time tartaric acid and its derivatives have been often used in chemistry due to their accessibility, enantiopurity, relatively low cost and presence of different functional groups which easily allow to modify the molecule. Many tartaric acid derivatives serve as catalysts in important stereoselective transformations such as Sharpless asymmetric epoxidation or asymmetric Rousch aryloboronation. In many others reactions tartaric acid have been employed as a chiral building block for natural products synthesis, highly functionalized molecules or ligand design such as well known TADDOL or its analogues. Its polar functional groups allow to form crystals with amines and aminoalcohols what is widely used for their enantiopurification and resolution. The relatively new subdiscipline is the use of tartaric acid in chiral recognition and chiral discrimination in nanochemistry and enantioselective chromatography. The other, recent applications of tartaric acid include functionalization of metal layers, antibacterial and antifungal activity among many others. The significance of tartaric acid is evident – since 2000, words “tartaric acid” or “tartrates” can be found in databases over four thousand times. Taking that into account this short review is concentrated on selected applications of tartaric acid and its derivatives in organic chemistry in recent several years.

Słowa kluczowe

kwas winowy winiany stereochemia synteza organiczna kataliza

tartaric acid tartrates stereochemistry organic synthesis catalysis

Wydawca

Polskie Towarzystwo Chemiczne

Czasopismo

Wiadomości Chemiczne

Rocznik

2013

Tom

[Z] 67, 5-6

Strony

495--519

Opis fizyczny

Bibliogr. 73 poz., rys., schem.

Twórcy

autor

Grajewski J.

jakub.grajewski@amu.edu.pl

Uniwersytet im. Adama Mickiewicza w Poznaniu, Wydział Chemii, Zakład Stereochemii Organicznej ul. Grunwaldzka 6, 60-760 Poznań

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Typ dokumentu

Bibliografia

Identyfikator YADDA

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