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Information Seminar Paper

Title

REGIOSELECTIVITY IN CHEMICAL REACTIONS, USING SHANNON INFORMATION ENTROPY

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  -

Abstract

 INTRODUCTION: DIELS-ALDER REACTIONS HAVE A SPECIAL IMPORTANCE IN ORGANIC CHEMISTRY. WHEN BOTH OF THE REAGENTS IN THIS REACTION ARE ASYMMETRICALLY SUBSTITUTED, REGIOSELECTIVITY IS OBSERVED. THE PATERNO-BÜCHI REACTION, THE FORMATION OF OXETANES VIA PHOTOCHEMICAL [2+2] CYCLOADDITION OF CARBONYL COMPOUNDS TO ALKENES, IS THE MOST GENERAL METHOD FOR THE SYNTHESIS OF FOUR-MEMBERED OXYGEN HETEROCYCLIC RINGS IN A REGIOSELECTIVE MANNER.

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    • Cite

    APA: Copy

    NOORIZADEH, S., & BEHZADI SAMANI, M.. (2013). REGIOSELECTIVITY IN CHEMICAL REACTIONS, USING SHANNON INFORMATION ENTROPY. IRANIAN PHYSICAL CHEMISTRY CONFERENCE. SID. https://sid.ir/paper/909546/en

    Vancouver: Copy

    NOORIZADEH S., BEHZADI SAMANI M.. REGIOSELECTIVITY IN CHEMICAL REACTIONS, USING SHANNON INFORMATION ENTROPY. 2013. Available from: https://sid.ir/paper/909546/en

    IEEE: Copy

    S. NOORIZADEH, and M. BEHZADI SAMANI, “REGIOSELECTIVITY IN CHEMICAL REACTIONS, USING SHANNON INFORMATION ENTROPY,” presented at the IRANIAN PHYSICAL CHEMISTRY CONFERENCE. 2013, [Online]. Available: https://sid.ir/paper/909546/en

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