Metal-free domino Cloke-Wilson rearrangement-hydration-dimerization of cyclopropane carbaldehydes: A facile access to oxybis(2-aryltetrahydrofuran) derivatives

Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/1948

Full metadata record

DC Field	Value	Language
dc.contributor.author	Dey, R.
dc.contributor.author	Rajput, S.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2021-07-01T17:00:06Z
dc.date.available	2021-07-01T17:00:06Z
dc.date.issued	2021-07-01
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/1948
dc.description.abstract	In this work, we have demonstrated a metal-free transformation of cyclopropane carbaldehydes to oxybis(2-aryltetrahydrofuran) derivatives via a domino Cloke-Wilson rearrangement-hydration-dimerization sequence. Commercially inexpensive p-toluene sulfonic acid (PTSA) was used as a Brønsted acid catalyst, and reactions were conducted in an open-flask. Detection of reaction intermediates were carried to get an insight into the reaction pathway.	en_US
dc.language.iso	en_US	en_US
dc.subject	Cyclopropanes	en_US
dc.subject	Metal-free	en_US
dc.subject	PTSA	en_US
dc.subject	Domino reaction	en_US
dc.subject	Oxybis(2-aryltetrahydrofuran) derivatives	en_US
dc.title	Metal-free domino Cloke-Wilson rearrangement-hydration-dimerization of cyclopropane carbaldehydes: A facile access to oxybis(2-aryltetrahydrofuran) derivatives	en_US
dc.type	Article	en_US
Appears in Collections:	Year-2020

Files in This Item:

File	Description	Size	Format
Fulltext.pdf		1.04 MB	Adobe PDF	View/Open Request a copy

DSpace JSPUI