Improved high-yield synthesis of polycyclic aromatic hydrocarbon amino tribenzoates, nucleophilic components for synthesis of diol epoxide-nucleoside adducts

Article abstract of DOI:10.1080/00397919408010618

This report describes an improved high-yield synthesis of amino tribenzoates derived through a trans-ring opening of diol epoxides. A significant difference in the relative reactivities of benzo[a]pyrene series-1 and series-2 diol epoxide diastereomers wi

Full text of DOI:10.1080/00397919408010618

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Improved High-Yield
Synthesis of Polycyclic
Aromatic Hydrocarbon Amino
Tribenzoates, Nucleophilic
Components for Synthesis
of Diol Epoxide-Nucleoside
Adducts
Mahesh K. Lakshman a , Surendrakumar Chaturvedi b
& Roland E. Lehr b
a Laboratory of Bioorganic Chemistry , NIDDK
National Institutes of Health , Bethesda, MD, 20892
b Department of Chemistry and Biochemistry , The
University of Oklahoma , Norman, OK, 73019
Published online: 23 Sep 2006.
To cite this article: Mahesh K. Lakshman , Surendrakumar Chaturvedi & Roland
E. Lehr (1994) Improved High-Yield Synthesis of Polycyclic Aromatic Hydrocarbon
Amino Tribenzoates, Nucleophilic Components for Synthesis of Diol Epoxide-
Nucleoside Adducts, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 24:20, 2983-2988, DOI:
10.1080/00397919408010618
To link to this article: http://dx.doi.org/10.1080/00397919408010618

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