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Studies on the cyclisation of two key allyl phenol intermediates of bromotyrosine based natural products

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dc.contributor.author Mallavadhani, U.V.
dc.contributor.author Narasimhan, K.
dc.date.accessioned 2018-10-01T12:22:06Z
dc.date.available 2018-10-01T12:22:06Z
dc.date.issued 2003
dc.identifier.citation Indian Journal Of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry, 42(1), 2003: 199-201
dc.identifier.issn 0376-4699
dc.identifier.uri http://ore.immt.res.in/handle/2018/1079
dc.description.abstract Cyclisation of two key allyl phenol intermediates viz. 2-allyl-6-bromo-4-formyl phenol 1 and 4-acetyl-2-allyl-6-bromo phenol 2 has been studied under a variety of acid catalysts. While mineral and organic acids did not yield any cyclic products, polyphosphoric acid and 70% perchloric acid affected the cyclisation upto 55-70%. Significantly the cationic montmorillonite clays have been used for the first time and found to affect the regioselective cyclisation and yielded the five membered coumarans in quantitative yields.
dc.language en
dc.publisher National Institute Of Science Communication And Information Resources - NISCAIR
dc.relation.isreferencedby SCI
dc.rights Copyright [2003]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subject Chemical Sciences
dc.title Studies on the cyclisation of two key allyl phenol intermediates of bromotyrosine based natural products
dc.type Journal Article
dc.affiliation.author CSIR-IMMT, Bhubaneswar 751013, Odisha, India


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