Asymmetric Assembly of Steroidal Tetracyclic Skeletons

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dc.contributor.author Gupta, Preeti
dc.contributor.author Panda, Gautam
dc.date.accessioned 2017-06-13T07:32:32Z
dc.date.available 2017-06-13T07:32:32Z
dc.date.issued 2014
dc.identifier.citation European Journal of Organic Chemistry, 2014, 36, 8004-8019 en
dc.identifier.uri http://hdl.handle.net/123456789/1701
dc.description.abstract Steroids have long played a vital role in the organic synthesis because of their unique structural design and associated biological properties. In recent years, asymmetric synthesis has emerged as a powerful tool for assembling the tetracyclic framework with high level of molecular diversity. This review summarizes the latest developments in the enantioselective syntheses of both natural and synthetic steroids incorporationg the carbocyclic skeleton. The approaches to the synthesis of steroids and related molecules are based primarily on the use of chiral starting materials, the employment of reagent-controlled asymmetric induction assisted by chiral complexes, chiral Lewis acids or organocatalysts, or the utilisation of chiral auxiliaries. en
dc.format.extent 803139 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI communication no 8786 en
dc.subject Steroids en
dc.subject Asymmetric synthesis en
dc.subject Chiral pool en
dc.subject Synthetic methods en
dc.subject Total Synthesis en
dc.title Asymmetric Assembly of Steroidal Tetracyclic Skeletons en
dc.type Article en


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