Literature DB >> 21434691

Stereoselective synthesis of both enantiomers of rugulactone.

Dietrich Böse1, Enrique Fernández, Jörg Pietruszka.   

Abstract

The stereoselective total synthesis of both enantiomers of rugulactone 1 has been completed by applying enantioselective allyl additions as key steps. Two different strategies based on highly stable and enantiomerically pure α-substituted allylboronic esters 2 and 3 were performed starting from boronic ester 4.
© 2011 American Chemical Society

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Year:  2011        PMID： 21434691     DOI： 10.1021/jo2004583

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


  5 in total

1.  Palladium-catalyzed synthesis and isolation of functionalized allylboronic acids: selective, direct allylboration of ketones.

Authors:  Mihai Raducan; Rauful Alam; Kálmán J Szabó
Journal:  Angew Chem Int Ed Engl       Date:  2012-11-19       Impact factor: 15.336

Review 2.  Recent Advances in the Stereoselective Total Synthesis of Natural Pyranones Having Long Side Chains.

Authors:  Satya Kumar Avula; Biswanath Das; Rene Csuk; Ahmed Al-Rawahi; Ahmed Al-Harrasi
Journal:  Molecules       Date:  2020-04-20       Impact factor: 4.411

3.  An Efficient Chemoenzymatic Approach towards the Synthesis of Rugulactone.

Authors:  Theodore Tyrikos-Ergas; Vasileios Giannopoulos; Ioulia Smonou
Journal:  Molecules       Date:  2018-03-12       Impact factor: 4.411

4.  Synthesis of a simplified triazole analogue of pateamine A.

Authors:  A Hemi Cumming; Sarah L Brown; Xu Tao; Claire Cuyamendous; Jessica J Field; John H Miller; Joanne E Harvey; Paul H Teesdale-Spittle
Journal:  Org Biomol Chem       Date:  2016-05-16       Impact factor: 3.876

5.  A facile stereoselective total synthesis of (R)-rugulactone.

Authors:  B Narasimha Reddy; R P Singh
Journal:  ISRN Org Chem       Date:  2014-03-30
  5 in total

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