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Linear dialdehydes as promising substrates for aminocatalyzed transformation

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dc.contributor.author Kumar, Indresh
dc.date.accessioned 2021-10-27T04:27:52Z
dc.date.available 2021-10-27T04:27:52Z
dc.date.issued 2015
dc.identifier.uri https://pubs.rsc.org/en/content/articlelanding/2015/ob/c4ob01805b
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3172
dc.description.abstract Organocatalytic domino reactions involving amine activation of carbonyl compounds have become the latest chemical technology towards the design and development of useful synthetic methods. In this direction, linear dialdehydes such as succinaldehyde, glutaraldehyde, and other homologous compounds have attracted considerable attention as suitable substrates for amine catalyzed transformations. Due to their unique structural features, dialdehydes can easily engage in recreation of cascade/tandem transformations for the synthesis of valuable natural products and drug molecules. In this review article we discuss the current scenario and potential applications of linear dialdehydes as adequate synthetic substrates for amine catalyzed transformations to access biologically important complex scaffolds. en_US
dc.language.iso en en_US
dc.publisher RSC en_US
dc.subject Chemistry en_US
dc.subject Dialdehydes en_US
dc.subject Aminocatalyzed en_US
dc.title Linear dialdehydes as promising substrates for aminocatalyzed transformation en_US
dc.type Article en_US


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