Please use this identifier to cite or link to this item:
http://hdl.handle.net/2080/2768
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sarkar, Debayan | - |
dc.date.accessioned | 2017-10-10T05:09:30Z | - |
dc.date.available | 2017-10-10T05:09:30Z | - |
dc.date.issued | 2017-08 | - |
dc.identifier.citation | RSC Seminar, Kolkata, India, 18 August, 2017. | en_US |
dc.identifier.uri | http://hdl.handle.net/2080/2768 | - |
dc.description | Copyright of this document is with proceedings publisher. | en_US |
dc.description.abstract | At the heart of any chemical synthesis of a natural product or designed small molecule is the need to orchestrate a series of chemical reactions to prepare and functionalize a carbon framework. The advent of transition-metal catalysis has provided chemists with a broad range of new tools to forge C−C and C−X bonds and has resulted in a paradigm shift in synthetic strategy planning. The ruthenium catalysed C−C coupling reaction of propargyl alcohol and Michael acceptor has been demonstrated an enabling methodology for synthesis o α,β-unsaturated ketones as a single geometrical isomers of high yield in an atom-economical fashion. The synthesized α,β-unsaturated ketones are the precursor of poly-substituted piperidones and hexahydroisoquilininones which are the central backbone of many biologically active natural products and pharmaceutical drugs. | en_US |
dc.subject | Ruthenium Catalysed | en_US |
dc.subject | Atom-Economic Transformations | en_US |
dc.title | Ruthenium-Catalysed Atom-Economic Transformations | en_US |
dc.type | Article | en_US |
Appears in Collections: | Conference Papers |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2017_RSCS_DSarkar_Ruthenium.pdf | Scientific lecturer | 424.83 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.