An efficient and rapid chalcogenide-Morita-Baylis-Hillman process promoted by TBDMSOTf and a thiolane

dc.contributor.author Rao, Jamjanam Srivardhana
dc.contributor.author Brière, Jean François
dc.contributor.author Metzner, Patrick
dc.contributor.author Basavaiah, Deevi
dc.date.accessioned 2022-03-27T09:02:09Z
dc.date.available 2022-03-27T09:02:09Z
dc.date.issued 2006-05-22
dc.description.abstract The ability of the combination of sulfide/TBDMSOTf to promote a chalcogenide-Morita-Baylis-Hillman reaction is reported. The original Michael-Mukaiyama-retroaldol sequence took place and furnished the MBH adducts from the corresponding enones and acetals. This one step process could be performed smoothly at low temperatures (-20 to -50 °C) and is rapidly completed within a few hours. © 2006 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.47(21)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2006.03.070
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403906005260
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12305
dc.subject Acetal
dc.subject Chalcogenide-Morita-Baylis-Hillman
dc.subject Enone
dc.subject Sulfide
dc.subject TBDMSOTf
dc.title An efficient and rapid chalcogenide-Morita-Baylis-Hillman process promoted by TBDMSOTf and a thiolane
dc.type Journal. Article
dspace.entity.type
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