Literature DB >> 11829598

Synthesis of (E)-1,2-divinyl-1,2-diethynylethene (DVDEE) via the palladium-catalyzed reaction of conjugated diynes. A new building block for molecular scaffolding.

Drexel H Camacho1, Shinichi Saito, Yoshinori Yamamoto.   

Abstract

Conjugated diynes undergo dimerization in the presence of acetic acid and catalytic amounts of Pd(PPh3)4. The unprecedented reaction gives a novel chromophore containing the (E)-1,2-divinyl-1.2-diethynylethene (DVDEE) module, which is a potentially viable building block for acetylenic scaffolding.

Entities:  

Year:  2002        PMID: 11829598     DOI: 10.1021/ja017626p

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Selectivity in the ruthenium-catalyzed alder ene reactions of di- and triynes.

Authors:  Eun Jin Cho; Daesung Lee
Journal:  J Am Chem Soc       Date:  2007-05-08       Impact factor: 15.419

2.  Controlling the conformational changes in donor-acceptor [4]-dendralenes through intramolecular charge-transfer processes.

Authors:  Alexander L Kanibolotsky; John C Forgie; Greg J McEntee; M Munsif A Talpur; Peter J Skabara; Thomas D J Westgate; Joseph J W McDouall; Michael Auinger; Simon J Coles; Michael B Hursthouse
Journal:  Chemistry       Date:  2009-11-02       Impact factor: 5.236

  2 in total

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