Literature DB >> 24784888

Diastereoselective construction of trans-fused octalone framework via ruthenium-porphyrin-catalyzed cycloaddition.

Takuma Terada1, Takuya Kurahashi, Seijiro Matsubara.   

Abstract

Lewis acid catalyzed cycloaddition of cyclohexenone and butadiene affords trans-fused octalone with high regio- and diastereoselectivity. The use of the ruthenium porphyrin complex as the Lewis acid catalyst is key to the reaction. The cycloaddition proceeds in toluene with 1 mol % of the ruthenium catalyst at 25 °C.

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Year:  2014        PMID: 24784888     DOI: 10.1021/ol500625r

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Rhodium(i)-catalyzed asymmetric [4 + 2] cycloaddition reactions of 2-alkylenecyclobutanols with cyclic enones through C-C bond cleavage: efficient access to trans-bicyclic compounds.

Authors:  Xinxin Zheng; Rui Guo; Guozhu Zhang; Dayong Zhang
Journal:  Chem Sci       Date:  2018-01-08       Impact factor: 9.825

  1 in total

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