A direct access to a potential LTB4-antagonist, SM-9064, via disilyl derivatives

Article abstract of DOI:10.1080/00397919308009765

The synthesis of SM-9064, a potential LTB₄ antagonist, which is effective in some types of inflammation, has been easily achieved in a few steps by electrophilic substitution reactions between (1E,3E,5E)-1,6-bis(trimethylsilyl)-1,3,5-hexatriene

Full text of DOI:10.1080/00397919308009765

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Synthetic Communications: An
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Organic Chemistry
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A Direct Access to a Potential
LTB4-Antagonist, SM-9064, via,
Disilyl Derivatives
Vito Fiandanese a & Angela Punzi a
a Centro CNR di Studio sulle Metodologie Innovative
di Sintesi Organiche, Dipartimento di Chimica,
Università , via Amendola 173, 70126, Bari, Italy
Published online: 23 Sep 2006.
To cite this article: Vito Fiandanese & Angela Punzi (1993) A Direct Access
to a Potential LTB4-Antagonist, SM-9064, via, Disilyl Derivatives, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:2, 173-182, DOI: 10.1080/00397919308009765
To link to this article: http://dx.doi.org/10.1080/00397919308009765
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