Literature DB >> 17711346

Implications for the existence of a heptasulfur linkage in natural o-benzopolysulfanes.

David Aebisher1, Edyta M Brzostowska, Nahed Sawwan, Rafael Ovalle, Alexander Greer.   

Abstract

Natural o-benzopolysulfanes are often thought to exist as either the trisulfane or pentasulfane; the nomenclature has evolved around such notions. No study makes reference to the possible existence of natural o-benzoheptasulfanes. The work performed here indicates that a facile equilibration takes place between the tri-, penta-, and heptasulfanes (o-C(6)H(4)S(3), o-C(6)H(4)S(5), and o-C(6)H(4)S(7)) in solution. In these simpler (unnatural) compounds, the number of sulfur atoms can be established unequivocally from their independent syntheses. The o-benzopolysulfanes, even after purification, yield mixtures of compounds in solution. A similar equilibration may be anticipated for the corresponding natural products.

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Year:  2007        PMID: 17711346     DOI: 10.1021/np070108t

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  1 in total

1.  Synthesis, characterization, mechanism of decomposition, and antiproliferative activity of a class of PEGylated benzopolysulfanes structurally similar to the natural product varacin.

Authors:  Adaickapillai Mahendran; Angela Vuong; David Aebisher; Yaqiong Gong; Robert Bittman; Gilbert Arthur; Akira Kawamura; Alexander Greer
Journal:  J Org Chem       Date:  2010-08-20       Impact factor: 4.354

  1 in total

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