Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/55437
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dc.contributor.authorChowhan, L Raju-
dc.contributor.authorRaghavan, Sadagopan-
dc.date.accessioned2020-10-05T08:55:57Z-
dc.date.available2020-10-05T08:55:57Z-
dc.date.issued2020-08-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/55437-
dc.description1199-1205en_US
dc.description.abstractA stereoselective synthesis towards (+)-trans-kumausyne is disclosed. The key steps of the synthesis include stereoselective C-C formation employing vinylogous Mukaiyama type reaction of an α-chloro sulfide with 2-trimethylsiloxy furan and base-catalyzed isomerization followed by intramolecular oxa-Michael reaction.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(08) [August 2020]en_US
dc.subjectα-Chloro sulfideen_US
dc.subjectMukaiyama type reactionen_US
dc.subjectOxa-Michael additionen_US
dc.subject(+)-trans-Kumausyneen_US
dc.subject2-trimethylsiloxy furanen_US
dc.titleStereoselective synthesis towards (+)-trans-kumausyne employing vinylogous Mukaiyama type reaction on an α-chloro sulfideen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.59B(08) [August 2020]

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