Developing Organocatalysts For Enantioselective Aldol-Type Reactions

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14160%2F23%3A00132223" target="_blank" >RIV/00216224:14160/23:00132223 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Developing Organocatalysts For Enantioselective Aldol-Type Reactions

Popis výsledku v původním jazyce

From a broader perspective, aldol-type reactions encompass a plethora of fundamental chemical transformations embodied by the addition of compounds with active hydrogen to molecules bearing a carbonyl or extended carbonyl functionality. Despite the relative attractiveness of chiral aldol units for the construction of bioactive scaffolds, performing these reactions in an enantioselective fashion and downstream chemistry of enantioenriched aldol adducts are both far from trivial. Most products are prone to retro-aldol cleavage and elimination, resulting in a possible undesired epimerization or dehydration during isolation or a subsequent reaction sequence. Furthermore, lower aliphatic aldehydes are gases or low-boiling liquids requiring special procedures for handling. The above aspects represented just a fraction of the challenges to achieving high enantioselectivity for aldol-type processes while developing and screening chiral bifunctional hydrogen bond donor organocatalysts in our group.

Název v anglickém jazyce

Developing Organocatalysts For Enantioselective Aldol-Type Reactions

Popis výsledku anglicky

From a broader perspective, aldol-type reactions encompass a plethora of fundamental chemical transformations embodied by the addition of compounds with active hydrogen to molecules bearing a carbonyl or extended carbonyl functionality. Despite the relative attractiveness of chiral aldol units for the construction of bioactive scaffolds, performing these reactions in an enantioselective fashion and downstream chemistry of enantioenriched aldol adducts are both far from trivial. Most products are prone to retro-aldol cleavage and elimination, resulting in a possible undesired epimerization or dehydration during isolation or a subsequent reaction sequence. Furthermore, lower aliphatic aldehydes are gases or low-boiling liquids requiring special procedures for handling. The above aspects represented just a fraction of the challenges to achieving high enantioselectivity for aldol-type processes while developing and screening chiral bifunctional hydrogen bond donor organocatalysts in our group.

Druh

O - Ostatní výsledky

CEP obor

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OECD FORD obor

30104 - Pharmacology and pharmacy

Projekt

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Návaznosti

S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2023

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů