Literature DB >> 16623581

New method based on 1-(trimethysilyl)alk-1-yne to prepare 1,4-skipped diynes.

Florian Montel1, Renaud Beaudegnies, Jilali Kessabi, Benjamin Martin, Eric Muller, Sebastian Wendeborn, Pierre M J Jung.   

Abstract

[reaction: see text] We have developed a novel reaction between a terminal TMS-alkyne and a propargyl halide in the presence of a fluoride source and a catalytic amount of copper iodide to prepare 1,4-skipped diynes with good yields and in mild conditions. We have shown that this reaction also works very well with germanium and tin derivatives as an alternative to silicon. This new method can be useful for the synthesis of polyunsaturated fatty acids.

Entities:  

Year:  2006        PMID: 16623581     DOI: 10.1021/ol0604670

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


  1 in total

1.  Unified total synthesis of the natural products endiandric acid A, kingianic acid E, and kingianins A, D, and F.

Authors:  S L Drew; A L Lawrence; M S Sherburn
Journal:  Chem Sci       Date:  2015-05-07       Impact factor: 9.825

  1 in total

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