Literature DB >> 10814202

Cyclization into hydrindanones using samarium diiodide

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Abstract

Samarium(II) iodide has been employed to promote vinylogous pinacol coupling reaction of aldehyde onto alpha,beta-unsaturated ketones. The diastereoselectivity of 6-endo products was changed by addition of a proton source and/or HMPA and by the reaction temperature. The cyclization reactions described herein provide a general approach to the syntheses of 3,3-dimethylhydrindanes with a cis-relationship between the OH at C-4 and the proton at C-3a with good diastereoselectivity and under mild reaction conditions.

Entities:  

Year:  2000        PMID: 10814202     DOI: 10.1021/jo9918450

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


  1 in total

1.  Cyclizations producing hydrindanones with two methyl groups at the juncture positions mediated by samarium diiodide and electrolysis.

Authors:  Masakazu Sono; Natsuko Ise; Tsutomu Shoji; Motoo Tori
Journal:  Molecules       Date:  2012-09-13       Impact factor: 4.411

  1 in total

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