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β‐Lactam‐Synthon Interceded Diastereoselective Synthesis of 2‐Azido‐γ‐amino Alcohols with Subsequent Transformations to Functionally Enriched Heterocycles
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2018 (English)In: ChemistrySelect, E-ISSN 2365-6549, Vol. 3, no 17, p. 4764-4767Article in journal (Refereed) 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.

Place, publisher, year, edition, pages
John Wiley & Sons, 2018. Vol. 3, no 17, p. 4764-4767
Keywords [en]
2-azido-gamma-amino alcohol, 3-azido-azetidine, cis-oxazinane, intramolecular click chemistry, beta-lactam-synthon protocol
National Category
Organic Chemistry
Identifiers
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
Available from: 2018-05-30 Created: 2018-05-30 Last updated: 2024-08-30Bibliographically approved

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Singh, Pardeep

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