Literature DB >> 16808536

Novel and efficient syntheses of (-)-methyl 4-epi-shikimate and 4,5-epoxy-quinic and -shikimic acid derivatives as key precursors to prepare new analogues.

Laura Sánchez-Abella1, Susana Fernández, Nuria Armesto, Miguel Ferrero, Vicente Gotor.   

Abstract

We have developed simple methods that provide a rapid entry into the synthesis of a series of quinate and shikimate analogues, including (-)-methyl 4-epi-shikimate and the 4,5-epoxy analogues of the parent acids. Epoxy derivatives of quinic and shikimic acids were converted into methyl scyllo-quinate and (+)-methyl 3-epi-shikimate, respectively, by processes involving a regio- and stereoselective epoxide ring opening. The strategies described take place through short, high-yield reaction sequences.

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Year:  2006        PMID: 16808536     DOI: 10.1021/jo0606249

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Synthesis of the Naturally Occurring (-)-1,3,5-Tri-O-Caffeoylquinic Acid.

Authors:  Kay M Brummond; Jolie E Deforrest
Journal:  Synlett       Date:  2009-02-11       Impact factor: 2.454

2.  Generation of aroE overexpression mutant of Bacillus megaterium for the production of shikimic acid.

Authors:  Saptarshi Ghosh; Uttam Chand Banerjee
Journal:  Microb Cell Fact       Date:  2015-05-17       Impact factor: 5.328

3.  Gram-scale carbasugar synthesis via intramolecular seleno-Michael/aldol reaction.

Authors:  Piotr Banachowicz; Szymon Buda
Journal:  RSC Adv       Date:  2019-04-26       Impact factor: 4.036

  3 in total

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