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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/11024
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dc.contributor.authorSarkar, Debayanen_US
dc.date.accessioned2022-11-03T19:56:57Z-
dc.date.available2022-11-03T19:56:57Z-
dc.date.issued2022-
dc.identifier.citationSahoo, S. R., Das, B., Sarkar, D., & Reuter, H. (2022). Temperature-controlled chemoselective synthesis of multisubstituted 4-Alkynyl/trans 4-alkenyl coumarins. Journal of Organic Chemistry, doi:10.1021/acs.joc.2c00994en_US
dc.identifier.issn0022-3263-
dc.identifier.otherEID(2-s2.0-85139918467)-
dc.identifier.urihttps://doi.org/10.1021/acs.joc.2c00994-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/11024-
dc.description.abstractA temperature-controlled facile synthesis of multisubstituted 4-alkynyl/trans 4-alkenyl coumarins with a metal salt cascade approach is reported. H2O serves both as a nucleophile and hydrogen source. The presence of metal salt facilitates the reduction of alkyne. The present protocol bypasses the structural shortcomings of the existing Sonogashira and Heck coupling reactions. In addition, the obtained 2,3-disubstituted coumarins are readily transformed into 2,3-disubstituted dihydrocoumarins, which serve as important building blocks in organic transformations. © 2022 American Chemical Society. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceJournal of Organic Chemistryen_US
dc.titleTemperature-Controlled Chemoselective Synthesis of Multisubstituted 4-Alkynyl/trans 4-Alkenyl Coumarinsen_US
dc.typeJournal Articleen_US
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