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Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon

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dc.contributor.author Bhat, C.
dc.contributor.author Tilve, S.G.
dc.date.accessioned 2015-06-04T04:22:26Z
dc.date.available 2015-06-04T04:22:26Z
dc.date.issued 2014
dc.identifier.citation RSC Advances. 4(11); 2014; 5405-5452. en_US
dc.identifier.uri http://dx.doi.org/10.1039/c3ra44193h
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/3049
dc.description.abstract The present article describes the synthesis of a wide spectrum of natural products of the class pyrrolidines, pyrrolizidines and indolizidines using proline as a viable synthetic precursor. The review emphasizes the versatility of the basic unit of proline as a useful chiral synthon confined for the synthesis of only natural products of the above mentioned families. The vast coverage of the synthesis of these natural products is presented for a period from 1990 onwards. The synthesis of all ranges of alkaloids from simple to complex molecules is presented under the groups of alkaloids. en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.title Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon en_US
dc.type Journal article en_US
dc.identifier.impf y


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