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tert-Butyl 8-oxo-5-thia-2-azaspiro[3.4]octane-2-carboxylate 5,5-dioxide
Synonym(e):
2-Boc-8-oxo-5-thia-2-azaspiro[3.4]octane 5,5-dioxide
About This Item
Empfohlene Produkte
Form
solid
Funktionelle Gruppe
ketone
sulfone
Lagertemp.
2-8°C
SMILES String
O=C(CCS1(=O)=O)C21CN(C(OC(C)(C)C)=O)C2
InChI
1S/C11H17NO5S/c1-10(2,3)17-9(14)12-6-11(7-12)8(13)4-5-18(11,15)16/h4-7H2,1-3H3
InChIKey
YXFLECMRQFDZGN-UHFFFAOYSA-N
Anwendung
Synthesis of Novel Azaspiro[3.4]octanes as Multifunctional Modules in Drug Discovery
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Artikel
Spirocyclic modules containing four-membered rings are currently of growing interest to discovery chemists.
Verwandter Inhalt
The Carreira Research Group is focused on expanding and creating access to uncharted landscape in chemical space. In joint efforts with SpiroChem, Carreira develops innovative spirocyclic building blocks, seeking to make them available to the community at large. Molecules constructed from these building blocks take on unique three-dimensional profiles due to the underlying spirocyclic scaffold, enriched by the presence of diverse combinations of exit vectors as sites for functionalization. Importantly, the spirocyclic building blocks possess physicochemical properties useful in the drug discovery process. Thus, drug leads can be tuned through appending these subunits to the periphery of a given scaffold. Moreover, these compact modules represent a useful collection of unprecedented inputs for fragment-based libraries. In all applications, the inherent novelty of the structure affords researchers new opportunities to run wild in their designs and avenues to chemical space – with their imagination as the sole limitations. We are proud to partner in the efforts to make these building blocks widely available.
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