Lithium (R)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate
97%
- Product Code: 202663
CAS:
2173637-01-7
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| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Widely used in asymmetric synthesis, this compound serves as a chiral building block for the preparation of β-amino acids and other nitrogen-containing pharmaceuticals. Its strained aziridine ring undergoes regioselective ring-opening reactions with various nucleophiles, enabling the formation of complex, enantiomerically pure molecules. It is particularly valuable in the synthesis of protease inhibitors and bioactive compounds where stereochemistry is critical. The Boc-protecting group allows for easy deprotection under mild acidic conditions, making it compatible with multi-step synthetic sequences. Its stability and reactivity profile make it a preferred choice in medicinal chemistry for constructing chiral intermediates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | $352.94 |
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| 100mg | 10-20 days | $427.13 |
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| 250mg | 10-20 days | $872.28 |
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| 1g | 10-20 days | $3,034.44 |
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Lithium (R)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate
Widely used in asymmetric synthesis, this compound serves as a chiral building block for the preparation of β-amino acids and other nitrogen-containing pharmaceuticals. Its strained aziridine ring undergoes regioselective ring-opening reactions with various nucleophiles, enabling the formation of complex, enantiomerically pure molecules. It is particularly valuable in the synthesis of protease inhibitors and bioactive compounds where stereochemistry is critical. The Boc-protecting group allows for easy deprotection under mild acidic conditions, making it compatible with multi-step synthetic sequences. Its stability and reactivity profile make it a preferred choice in medicinal chemistry for constructing chiral intermediates.
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