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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, 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
Keyword [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: 000431625900030OAI: oai:DiVA.org:umu-148018DiVA, id: diva2:1211383
Available from: 2018-05-30 Created: 2018-05-30 Last updated: 2018-06-09Bibliographically approved

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Singh, Pardeep

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