Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/55774
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKotha, Sambasivarao-
dc.contributor.authorPulletikurti, Sunil-
dc.date.accessioned2020-12-08T05:31:25Z-
dc.date.available2020-12-08T05:31:25Z-
dc.date.issued2020-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/55774-
dc.description1875-1880en_US
dc.description.abstractHerein is reported a concise synthesis of spiro-annulated cyclobutane tetracyclic and pentacyclic derivatives by ketene addition, and ring-rearrangement metathesis (RRM) as key steps, starting with commercially available norbornadiene and dicyclopentadiene. The tetracyclic spiro-derivative contains a [5/5/4] core unit, which is the key building block to angular triquinanes synthesis. Whereas, the pentacyclic spiro-derivative contains a basic core skeleton of presilphiperfolanes, and other sesquiterpenoids.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.59B(12) December 2020]en_US
dc.subjectCyclobutaneen_US
dc.subjectSpirocyclicen_US
dc.subjectKetene additionen_US
dc.subjectMetathesisen_US
dc.subjectDechlorinationen_US
dc.titleSynthesis of spiro-annulated cyclobutane derivatives through ketene [2+2] cycloaddition and ring-rearrangement metathesisen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.59B(12) December 2020]

Files in This Item:
File Description SizeFormat 
IJCB 59B(12) 1875-1880.pdfMain Article222.47 kBAdobe PDFView/Open
IJCB 59B(12) 1875-1880_Suppl Data.pdfSupplementary Data2.61 MBAdobe PDFView/Open


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