Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3200
Title: Direct Organocatalytic Multicomponent Synthesis of Enantiopure γ‐Butyrolactones via Tandem Knoevenagel‐Michael‐Lactonization Sequence
Authors: KHOPADE, TUSHAR M.
SONAWANE, AMOL D.
ARORA, JYOTSNA S.
BHAT, RAMAKRISHNA G.
Dept. of Chemistry
Keywords: Direct Organocatalytic
Multicomponent Synthesis
Enantiopure-Butyrolactones
Lactonization Sequence
Straightforward protocol
2017
Issue Date: Nov-2017
Publisher: Wiley
Citation: Advanced Synthesis & Catalysis, 359(22), 3905-3910.
Abstract: An expedient and straightforward protocol is developed for the synthesis of highly enantiopure synthesis of γ‐butyrolactones. For the first time, one pot enantioselective organocatalytic multicomponent reaction (OMCR) is explored to construct functionalized butyrolactones without the use of pre‐functionalized substrates and expensive transition metals. The protocol is proved to be reproducible on a gram scale. Density functional theory (DFT) calculations strongly support the mechanism and were in close agreement with the observed high stereoselectivity.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3200
https://doi.org/10.1002/adsc.201701084
ISSN: 1615-4150
1615-4169
Appears in Collections:JOURNAL ARTICLES

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