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β‐Lactam‐Synthon Interceded Diastereoselective Synthesis of 2‐Azido‐γ‐amino Alcohols with Subsequent Transformations to Functionally Enriched Heterocycles
Vise andre og tillknytning
2018 (engelsk)Inngår i: ChemistrySelect, ISSN 2365-6549, Vol. 3, nr 17, s. 4764-4767Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The present manuscript explicates Boron‐dimethylsulfide‐promoted diastereoselective synthesis of 2‐azido‐γ‐amino alcohols using β‐lactam synthon protocol along with its utilization in the formation of diversely functionalized heterocycles having biological relevance. The developed protocol has the potential to surpass the typical drawbacks of conventional protocols.

sted, utgiver, år, opplag, sider
John Wiley & Sons, 2018. Vol. 3, nr 17, s. 4764-4767
Emneord [en]
2-azido-gamma-amino alcohol, 3-azido-azetidine, cis-oxazinane, intramolecular click chemistry, beta-lactam-synthon protocol
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Identifikatorer
URN: urn:nbn:se:umu:diva-148018DOI: 10.1002/slct.201800512ISI: 000431625900030Scopus ID: 2-s2.0-85046629396OAI: oai:DiVA.org:umu-148018DiVA, id: diva2:1211383
Tilgjengelig fra: 2018-05-30 Laget: 2018-05-30 Sist oppdatert: 2023-03-24bibliografisk kontrollert

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