(PDF) Iodocyclization of Diallyl-Dihydroxy Naphthalenes

Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using &Lt;i>N-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle

International Journal of Organic Chemistry

doi 10.4236/ijoc.2013.33022

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Date

January 1, 2013

Authors

Pradipta Kumar Basu

Amrita Ghosh

Publisher

Scientific Research Publishing, Inc,

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Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using &Lt;i>N</I>-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle

International Journal of Organic Chemistry

doi 10.4236/ijoc.2013.33022

Full Text

Abstract

Date

Authors

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Characterization of Six Categories of Systematic 2<sup><i>n</I>－(<i>n</I>－<i>k</I>)</Sup> Fractional Factorial Designs

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Solutions of the Exponential Equation &Lt;i>y</I><sup><i>x/Y</I></Sup> = &Lt;i>x</I> Or Ln<i>x</I>/&Lt;i>x</I> = Ln<i>y</I>/&Lt;i>y</I> And Fine Structure Constant

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Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using &Lt;i&gt;N&lt;/I&gt;-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle

International Journal of Organic Chemistry

doi 10.4236/ijoc.2013.33022

Full Text

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Characterization of Six Categories of Systematic 2&lt;sup&gt;&lt;i&gt;n&lt;/I&gt;－(&lt;i&gt;n&lt;/I&gt;－&lt;i&gt;k&lt;/I&gt;)&lt;/Sup&gt; Fractional Factorial Designs

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Solutions of the Exponential Equation &Lt;i&gt;y&lt;/I&gt;&lt;sup&gt;&lt;i&gt;x/Y&lt;/I&gt;&lt;/Sup&gt; = &Lt;i&gt;x&lt;/I&gt; Or Ln&lt;i&gt;x&lt;/I&gt;/&Lt;i&gt;x&lt;/I&gt; = Ln&lt;i&gt;y&lt;/I&gt;/&Lt;i&gt;y&lt;/I&gt; And Fine Structure Constant

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C ∕ N Ratio, Stable Isotope (&Lt;i&gt;δ&lt;/I&gt;&lt;sup&gt;13&lt;/Sup&gt;C, &Lt;i&gt;δ&lt;/I&gt;&lt;sup&gt;15&lt;/Sup&gt;N), and &Lt;i&gt;n&lt;/I&gt;-Alkane Patterns of Brown Mosses Along Hydrological Gradients of Low-Centred Polygons of the Siberian Arctic

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Regular Elements and Right Units of Semigroup &Lt;i&gt;B&lt;sub&gt;x&lt;/Sub&gt;&lt;/I&gt;(&lt;i&gt;D&lt;/I&gt;) Defined Semilattice &Lt;i&gt;D&lt;/I&gt; For Which &Lt;i&gt;V&lt;/I&gt;(&lt;i&gt;D&lt;/I&gt;,а)=Q ∈ &Amp;sum;&lt;sub&gt;3&lt;/Sub&gt;(&lt;i&gt;X&lt;/I&gt;,8)

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Iodocyclization of Diallyl-Dihydroxy Naphthalenes Using &Lt;i>N</I>-Iodosuccinimide vs Molecular Iodine in Aqueous Micelle

Characterization of Six Categories of Systematic 2<sup><i>n</I>－(<i>n</I>－<i>k</I>)</Sup> Fractional Factorial Designs

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Solutions of the Exponential Equation &Lt;i>y</I><sup><i>x/Y</I></Sup> = &Lt;i>x</I> Or Ln<i>x</I>/&Lt;i>x</I> = Ln<i>y</I>/&Lt;i>y</I> And Fine Structure Constant

&Lt;i>In Vitro</I> Antagonistic Activity of &Lt;i>Trichoderma Harzianum</I> And &Lt;i>Bacillus Amyloliquefaciens</I> Against &Lt;i>Colletotrichum Acutatum</I>

C ∕ N Ratio, Stable Isotope (&Lt;i>δ</I><sup>13</Sup>C, &Lt;i>δ</I><sup>15</Sup>N), and &Lt;i>n</I>-Alkane Patterns of Brown Mosses Along Hydrological Gradients of Low-Centred Polygons of the Siberian Arctic

Identification of &Lt;i>ebs1</I>, &Lt;i>lsm6</I> And &Lt;i>nup159</I> As Suppressors of &Lt;i>spt</I>10 Effects at &Lt;i>ADH</I>2 in &Lt;i>Saccharomyces Cerevisiae</I> Suggests Post-Transcriptional Defects Affect mRNA Synthesis

Regular Elements and Right Units of Semigroup &Lt;i>B<sub>x</Sub></I>(<i>D</I>) Defined Semilattice &Lt;i>D</I> For Which &Lt;i>V</I>(<i>D</I>,а)=Q ∈ &Amp;sum;<sub>3</Sub>(<i>X</I>,8)

Irreducible Representations of Algebraic Group &Lt;i>SL</I>(6,<i>K</I>) in Char<i>K</I> =3

Phytohormone-Induced Resistance Against &Lt;i>Xanthomonas Axonopodis</I> PV. &Lt;i>citri</I> In &Lt;i>Citrus Aurantifolia</I>