For more than 130 years since the first preparation by Reboul, oxetanes have largely remained neglected in medicinal chemistry. The unit of oxetane can trigger profound changes in aqueous solubility, lipophilicity, metabolic stability, and conformational preference when replacing the commonly employed functionalities such as gem-dimethyl or carbonyl groups. Of particular interest are the oxetanes substituted at the 3-position, since they remain none-chiral. At the moment, oxetane-containing building blocks flourish in medicinal chemistry and drug discovery.
- high chemical stability;
- high aqueous solubility;
- low lipophilicity;
- high metabolic stability;
- hydrogen-bond acceptor ability.
- less lipophilic and more metabolically stable than a gem-dimethyl group;
- replacement for a metabolically and chemically labile carbonyl group;
- metabolically-robust analogue of morpholine.
>200 oxetane-containing building blocks on gram scale in stock.
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- Silicon-Containing Building Blocks
- Epoxides for Drug Design
- Analogues of CF3-Pyridine for Drug Design
- Piperazine Bioisosteres for Drug Design
- Sugar-like Building Blocks for Drug Design
- Cyclic Sulfonamides for Drug Design
- Morpholine Bioisosteres for Drug Design
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- Saturated Bioisosteres of ortho-/meta-substituted Benzenes
- Saturated bioisosteres of para-substituted benzenes
- Sulfonyl fluorides (-SO2F)
- Oxetane-containing Building Blocks
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- Saturated Bioisosteres of Benzene
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- Unnatural Amino Acids
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