An efficient 1,3-dipolar cycloaddition between aromatic selenoaldehydes and nitrile oxides or nitrile imines: an easy access to selenium-containing five-membered heterocyclic ring system

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概要

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• 1,3-Dipolar cycloaddition between aromatic selenoaldehydes, generated by thermal retro Diels-Alder reaction of anthracene cycloadducts, and nitrile oxides or nitrile imines proceeded efficiently to give the corresponding [3+2] cycloadducts as a single isomer in good yields, being 1,4,2-oxaselenazoles or 1,3,4-selenadiazoles, respectively. © 2007 Elsevier Ltd. All rights reserved.

• Elsevierの論文
• 2007-03-00

著者

• Nakajima Tadashi

  Division Of Material Sciences Graduate School Of Natural Science And Technology Kanazawa University

関連論文

• Stereoselective Construction of 1,3-Diol Derivatives via Nucleophilic Reaction to β-Methoxyacylsilanes
• An efficient 1,3-dipolar cycloaddition between aromatic selenoaldehydes and nitrile oxides or nitrile imines: an easy access to selenium-containing five-membered heterocyclic ring system

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