Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3834
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAkhil, K R-
dc.contributor.authorBabu, S A-
dc.contributor.authorNitha, P R-
dc.contributor.authorJagadeesh, K-
dc.contributor.authorJubi, J-
dc.date.accessioned2021-10-27T06:40:49Z-
dc.date.available2021-10-27T06:40:49Z-
dc.date.issued2021-
dc.identifier.citationOrganic Letters; 23(5):1814-1819en_US
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.orglett.1c00219-
dc.identifier.urihttp://hdl.handle.net/123456789/3834-
dc.description.abstractWe have developed a metal-free, mild, and green synthetic route toward benzothieno[3,2-b]benzofurans by the annulation of 3-nitrobenzothiophene with phenols. The reaction was found to be general with a range of substituted phenols. In addition, we could extend the methodology for the synthesis of pentacenes and could demonstrate the synthesis in gram-scale. Moreover, we extended the strategy for the synthesis of benzothieno[2,3-b]benzofurans by starting from 2-nitrobenzothiophenes.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjecthydrocarbonsen_US
dc.subjectchemical reactionsen_US
dc.subjectaromatic compoundsen_US
dc.subjectannulationsen_US
dc.subjectethanolen_US
dc.titleSynthesis of Benzothienobenzofurans via Annulation of Electrophilic Benzothiophenes with Phenolsen_US
dc.typeArticleen_US
Appears in Collections:2021

Files in This Item:
File Description SizeFormat 
Synthesis of Benzothienobenzofurans via Annulation_AkhilKR_Organic Letters.pdf
  Restricted Access
1.23 MBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.